altLabel id comment label rgo:may_be_caused_by may_be_caused_by rgo:may_cause may_cause RGO:00000 GamutThing RGO:00000 retention of contrast in hypopharynx RGO:00001 retained material in hypopharynx RGO:00001 SNOMEDCT:447220009 RGO:00012 hematoma of neck RGO:00012 HP:0025289 SNOMEDCT:127086001 RGO:00013 cervical lymphadenopathy RGO:00013 DOID:1781 RGO:00016 thyroid neoplasm RGO:00016 SNOMEDCT:71363005 RGO:00020 cricopharyngeal achalasia RGO:00020 RGO:00021 idiopathic diffuse esophageal spasm RGO:00021 RADLEX:RID5258 SNOMEDCT:235634004 RGO:00026 presbyesophagus RGO:00026 progressive systemic sclerosis systemic sclerosis DOID:418 DOID:419 HP:0100324 ORDO:801 RADLEX:RID34592 SNOMEDCT:422801000 SNOMEDCT:89155008 RGO:00027 scleroderma RGO:00027 DOID:14183 RGO:00028 alcoholic neuropathy RGO:00028 American trypanosomiasis DOID:12140 RGO:00031 Chagas disease RGO:00031 DOID:8778 RADLEX:RID3475 SNOMEDCT:34000006 RGO:00034 Crohn disease RGO:00034 DOID:9743 SNOMEDCT:230572002 RGO:00035 diabetic neuropathy RGO:00035 DOID:9164 SNOMEDCT:235630008 RGO:00037 hypertensive lower esophageal sphincter RGO:00037 SNOMEDCT:68480001 RGO:00039 intramural diverticulosis of esophagus RGO:00039 SNOMEDCT:235628006 RGO:00042 nutcracker esophagus RGO:00042 ORDO:2978 RGO:00051 chronic idiopathic intestinal pseudo-obstruction RGO:00051 RGO:00056 air in esophagus RGO:00056 cardiospasm DOID:9164 HP:0002571 RADLEX:RID34582 SNOMEDCT:48531003 RGO:00057 achalasia RGO:00057 corrosive esophagitis RGO:00061 caustic esophagitis RGO:00061 HP:0100628 SNOMEDCT:414133009 RGO:00062 esophageal diverticulum RGO:00062 RGO:00067 cricopharyngeal muscle RGO:00067 HP:0100594 ICD10CM:Q39.4 RADLEX:RID34693 SNOMEDCT:19216006 RGO:00068 esophageal web RGO:00068 RADLEX:RID3798 RGO:00069 lymph node enlargement RGO:00069 RGO:00070 osteophyte of cervical spine RGO:00070 RADLEX:RID3749 SNOMEDCT:204676004 RGO:00076 ectopic gastric mucosa RGO:00076 RGO:00097 aortic knob RGO:00097 RGO:00100 anomalous innominate artery RGO:00100 SNOMEDCT:74561007 RGO:00101 aortic diverticulum RGO:00101 RGO:00104 azygos or hemiazygos vein dilatation RGO:00104 HP:0011588 ORDO:99079 SNOMEDCT:253657003 RGO:00105 cervical aortic arch RGO:00105 HP:0011590 ICD10CM:Q25.45 ORDO:99075 SNOMEDCT:10451007 RGO:00107 double aortic arch RGO:00107 DOID:8478 ICD10CM:A42 SNOMEDCT:11817007 RGO:00116 actinomycosis RGO:00116 RGO:00125 double-barrel esophagus RGO:00125 HP:0100681 SNOMEDCT:66865009 RGO:00127 esophageal duplication RGO:00127 RGO:00128 intraluminal diverticulum RGO:00128 RGO:00130 intramural esophageal pseudodiverticulosis RGO:00130 RADLEX:RID4823 RGO:00133 Killian-Jamieson diverticulum RGO:00133 mid esophageal diverticulum RGO:00136 diverticulum of mid esophagus RGO:00136 RGO:00139 congenital pulsion diverticulum RGO:00139 lower esophageal diverticulum RGO:00141 diverticulum of lower esophagus RGO:00141 lower Zenker diverticulum SNOMEDCT:30126008 RGO:00142 epiphrenic diverticulum RGO:00142 RGO:00146 diffuse diverticula of esophagus RGO:00146 RGO:00147 intramural esophageal diverticulosis RGO:00147 RGO:00149 solitary esophageal filling defect RGO:00149 RADLEX:RID3711 SNOMEDCT:128477000 SNOMEDCT:44132006 RGO:00158 abscess RGO:00158 SNOMEDCT:2099007 RGO:00159 angioma RGO:00159 DOID:3315 HP:0012032 RADLEX:RID4342 SNOMEDCT:46720004 SNOMEDCT:93163002 RGO:00161 lipoma RGO:00161 malignant melanoma DOID:1909 HP:0002861 RADLEX:RID34617 SNOMEDCT:2092003 RGO:00163 melanoma RGO:00163 RGO:00165 prolapsed gastric fold RGO:00165 RGO:00167 ulcer with edema RGO:00167 DOID:0050869 RADLEX:RID4225 SNOMEDCT:128859003 RGO:00168 villous adenoma RGO:00168 RGO:00180 web or diaphragm of esophagus RGO:00180 DOID:11656 ICD10CM:L12.1 ORDO:46486 SNOMEDCT:34250006 RGO:00181 benign mucous membrane pemphigoid RGO:00181 DOID:2730 ICD10CM:Q81 SNOMEDCT:61003004 RGO:00184 epidermolysis bullosa RGO:00184 GVHD GvH disease ICD10CM:D89.81 ORDO:39812 RADLEX:RID34756 SNOMEDCT:234646005 RGO:00185 graft-versus-host disease RGO:00185 RGO:00190 metastasis or direct spread from adjacent malignancy RGO:00190 RGO:00191 peptic esophageal ulcer RGO:00191 SNOMEDCT:235201007 RGO:00193 sclerotherapy of esophageal varices RGO:00193 Z-E syndrome DOID:0050782 HP:0002044 ICD10CM:E16.4 ORDO:913 SNOMEDCT:53132006 RGO:00194 Zollinger-Ellison syndrome RGO:00194 RGO:00195 esophageal wall thickening RGO:00195 DOID:799 RADLEX:RID3366 SNOMEDCT:128060009 SNOMEDCT:12856003 RGO:00202 varices RGO:00202 DOID:9206 HP:0100580 RADLEX:RID5271 SNOMEDCT:302914006 RGO:00203 Barrett esophagus RGO:00203 RGO:00205 papillomatosis of esophagus RGO:00205 RGO:00206 peptic esophageal ulcer with edema RGO:00206 DOID:1107 HP:0011459 ORDO:70482 RGO:00208 esophageal carcinoma RGO:00208 RGO:00211 intubation esophagitis RGO:00211 RGO:00214 acute alcoholic esophagitis RGO:00214 RGO:00215 benign mucous pemphigoid RGO:00215 DOID:13922 ICD10CM:K20.0 ORDO:73247 RADLEX:RID3444 SNOMEDCT:235599003 RGO:00216 eosinophilic esophagitis RGO:00216 SNOMEDCT:235605005 RGO:00219 radiation esophagitis RGO:00219 RGO:00225 widespread irregular esophageal mucosa RGO:00225 RADLEX:RID5213 RGO:00227 glycogenic acanthosis RGO:00227 DOID:3138 HP:0000956 ICD10CM:L83 ORDO:924 RADLEX:RID3789 SNOMEDCT:402599005 RGO:00231 acanthosis nigricans RGO:00231 SNOMEDCT:50584008 RGO:00235 ectopic sebaceous glands RGO:00235 RGO:00236 esophagitis cystica RGO:00236 RGO:00237 feline esophagus RGO:00237 RADLEX:RID3810 SNOMEDCT:274134003 SNOMEDCT:50978000 RGO:00240 leukoplakia RGO:00240 RGO:00241 lymph follicles RGO:00241 RGO:00243 esophageal plaques RGO:00243 peptic esophagitis DOID:13976 ICD10CM:K21.0 RADLEX:RID3441 SNOMEDCT:266433003 RGO:00246 reflux esophagitis RGO:00246 varices of esophagus DOID:112 HP:0002040 ICD10CM:I85 ICD10CM:I85.0 SNOMEDCT:28670008 RGO:00249 esophageal varices RGO:00249 RGO:00255 esophageal lesion in a child RGO:00255 DOID:9182 ICD10CM:L10 SNOMEDCT:65172003 RGO:00267 pemphigus RGO:00267 DOID:12234 SNOMEDCT:54051005 RGO:00272 cascade stomach RGO:00272 RGO:00278 absent hemidiaphragm RGO:00278 RADLEX:RID5426 SNOMEDCT:235677003 SNOMEDCT:50568007 RGO:00284 bezoar RGO:00284 DOID:305 HP:0030731 RADLEX:RID4247 SNOMEDCT:68453008 RGO:00286 carcinoma RGO:00286 SNOMEDCT:19387007 RGO:00287 ectopic pancreas RGO:00287 HP:0004398 RADLEX:RID5039 SNOMEDCT:13200003 RGO:00295 peptic ulcer RGO:00295 enteric cyst RADLEX:RID3906 RGO:00299 duplication cyst RGO:00299 RGO:00300 fundic gland polyposis RGO:00300 SNOMEDCT:197047007 RGO:00304 jejunogastric intussusception RGO:00304 RGO:00307 prolapse of esophageal mucosa RGO:00307 RGO:00309 tumefactive extramedullary hematopoiesis RGO:00309 RGO:00321 diverticulum of gastric fundus RGO:00321 RGO:00325 hiatal hernia with esophagogastric herniation RGO:00325 RADLEX:RID3750 SNOMEDCT:38831007 RGO:00332 splenosis RGO:00332 ICD10CM:K65.1 RADLEX:RID3713 SNOMEDCT:52478002 RGO:00333 subphrenic abscess RGO:00333 SNOMEDCT:397825006 RGO:00334 gastric ulceration RGO:00334 carcinoid tumor HP:0100570 RADLEX:RID4246 SNOMEDCT:189607006 SNOMEDCT:81622000 RGO:00339 carcinoid RGO:00339 SNOMEDCT:196740009 RGO:00341 corrosive gastritis RGO:00341 RGO:00342 Cryptosporidium antritis RGO:00342 DOID:4030 RADLEX:RID3460 SNOMEDCT:66329006 RGO:00343 eosinophilic gastritis RGO:00343 hypertrophic gastropathy DOID:8757 HP:0005246 ORDO:2494 SNOMEDCT:60002000 RGO:00345 Ménétrier disease RGO:00345 SNOMEDCT:19750001 RGO:00347 pseudolymphoma RGO:00347 DOID:4029 RADLEX:RID3453 SNOMEDCT:1086791000119100 RGO:00350 erosive gastritis RGO:00350 DOID:3686 HP:0005202 RGO:00353 Helicobacter pylori infection RGO:00353 RGO:00357 postoperative gastritis RGO:00357 RGO:00365 postoperative stomach RGO:00365 RGO:00367 diffuse cystic gastric disease RGO:00367 RGO:00379 stenosing antral gastritis RGO:00379 RGO:00383 idiopathic gastritis RGO:00383 RGO:00384 intramural gastric hematoma RGO:00384 SNOMEDCT:89499009 RGO:00389 perigastric adhesions RGO:00389 SNOMEDCT:49781004 RGO:00390 phlegmonous gastritis RGO:00390 RGO:00392 postradiation or postfreezing gastritis RGO:00392 RADLEX:RID3455 RGO:00394 antral gastritis RGO:00394 RGO:00397 peptic ulcer scarring RGO:00397 DOID:12072 RADLEX:RID4815 SNOMEDCT:335002 RGO:00399 pylorospasm RGO:00399 RGO:00400 aberrant pancreatic tissue RGO:00400 RGO:00401 adhesions RGO:00401 RGO:00402 antral diaphragm or web RGO:00402 RGO:00405 duplication cyst of stomach RGO:00405 RADLEX:RID1631 SNOMEDCT:18692006 RGO:00406 gastroenterostomy RGO:00406 RGO:00411 combined gastric antral and duodenal disease RGO:00411 RGO:00412 carcinoma of stomach extending to involve duodenum RGO:00412 DOID:4031 ORDO:2070 RADLEX:RID3462 SNOMEDCT:359804008 RGO:00416 eosinophilic gastroenteritis RGO:00416 obstruction of stomach DOID:3122 RADLEX:RID4967 RGO:00418 gastric outlet obstruction RGO:00418 DOID:0060850 HP:0001734 ICD10CM:Q45.1 ORDO:675 SNOMEDCT:40315008 RGO:00426 annular pancreas RGO:00426 HP:0011139 RGO:00428 gastric duplication RGO:00428 RGO:00433 proximal small bowel obstruction RGO:00433 RGO:00455 tracheoesophageal fistula with esophageal atresia RGO:00455 RGO:00462 necrotizing gastroenterocolitis RGO:00462 RGO:00463 peptic ulcer with intramural perforation RGO:00463 RGO:00464 perforated appendicitis RGO:00464 RGO:00465 pneumatosis cystoides RGO:00465 RGO:00467 gastrocolic or gastroduodenocolic fistula RGO:00467 DOID:9180 SNOMEDCT:235747003 RGO:00473 amebic colitis RGO:00473 SNOMEDCT:16121001 RGO:00476 marginal ulcer RGO:00476 DOID:13258 ICD10CM:A01.0 SNOMEDCT:4834000 RGO:00478 typhoid fever RGO:00478 RGO:00479 increased retrogastric or retroduodenal space RGO:00479 HP:0001541 ICD10CM:R18 RADLEX:RID1541 SNOMEDCT:389026000 RGO:00480 ascites RGO:00480 DOID:899 HP:0100890 ICD10CM:Q44.4 RADLEX:RID3896 SNOMEDCT:440471007 RGO:00488 choledochal cyst RGO:00488 HP:0005200 ORDO:49041 RADLEX:RID3825 SNOMEDCT:49120005 RGO:00493 retroperitoneal fibrosis RGO:00493 RGO:00495 coloduodenal apposition RGO:00495 RGO:00504 papilla of Vater enlargement RGO:00504 RGO:00507 superior mesenteric artery compression RGO:00507 SNOMEDCT:84233008 RGO:00510 pericholecystic abscess RGO:00510 RGO:00514 duodenal diverticulitis RGO:00514 SNOMEDCT:262843005 RGO:00515 duodenal hematoma RGO:00515 RGO:00522 solitary intrinsic duodenal mass RGO:00522 RGO:00529 prolapsed gastric mucosa or polyp RGO:00529 RGO:00532 carcinoma of duodenum or ampulla RGO:00532 RGO:00535 gallstone impaction at papilla RGO:00535 RGO:00537 mesenteric or celiac artery collateral RGO:00537 RADLEX:RID4336 SNOMEDCT:235700007 RGO:00542 Brunner gland hyperplasia RGO:00542 RGO:00543 heterotopic gastric mucosa RGO:00543 RGO:00546 prolapsed gastric mucosa RGO:00546 DOID:456 ICD10CM:B77 RADLEX:RID34685 SNOMEDCT:2435008 RGO:00547 ascariasis RGO:00547 DOID:6225 ORDO:2930 SNOMEDCT:76304001 RGO:00550 Cronkhite-Canada syndrome RGO:00550 DOID:350 HP:0100495 ICD10CM:Q82.2 ORDO:2467 SNOMEDCT:125541005 RGO:00553 mastocytosis RGO:00553 RADLEX:RID5277 SNOMEDCT:81704009 RGO:00558 sprue RGO:00558 CF mucoviscidosis DOID:1485 ICD10CM:E84 ORDO:586 RADLEX:RID34638 SNOMEDCT:190905008 RGO:00559 cystic fibrosis RGO:00559 DOID:8643 ICD10CM:K29.8 RADLEX:RID3410 SNOMEDCT:72007001 RGO:00562 duodenitis RGO:00562 DOID:750 SNOMEDCT:13200003 RGO:00567 peptic ulcer disease RGO:00567 DOID:1949 HP:0001082 ICD10CM:K81 RADLEX:RID3394 SNOMEDCT:76581006 RGO:00570 cholecystitis RGO:00570 RGO:00571 corrosive disease RGO:00571 ICD10CM:K52.81 RGO:00573 eosinophilic enteritis RGO:00573 DOID:8476 ORDO:3452 RADLEX:RID5281 SNOMEDCT:41545003 RGO:00582 Whipple disease RGO:00582 RADLEX:RID4817 SNOMEDCT:31113003 RGO:00584 diverticulum RGO:00584 SNOMEDCT:254570009 RGO:00587 carcinoma of duodenum RGO:00587 SNOMEDCT:16010007 RGO:00588 duodenocolic fistula RGO:00588 RGO:00591 intramural duodenal pseudodiverticulosis RGO:00591 RGO:00594 duodenal narrowing or obstruction RGO:00594 SMA syndrome Wilkie syndrome arteriomesenteric duodenal compression DOID:3557 SNOMEDCT:197006009 RGO:00599 superior mesenteric artery syndrome RGO:00599 RGO:00600 aorticoduodenal fistula RGO:00600 RGO:00601 gallstone impaction RGO:00601 RGO:00605 midgut volvulus with malrotation RGO:00605 RGO:00608 preduodenal portal vein RGO:00608 RGO:00610 idiopathic pseudo-obstruction RGO:00610 RADLEX:RID4902 RGO:00623 paraduodenal hernia RGO:00623 RGO:00629 duodenal dilatation without obstruction RGO:00629 SNOMEDCT:79389008 RGO:00639 thiamine deficiency neuropathy RGO:00639 RGO:00640 abnormal small bowel position RGO:00640 RADLEX:RID4905 RGO:00643 lesser sac hernia RGO:00643 RADLEX:RID4918 SNOMEDCT:290187002 RGO:00650 spigelian hernia RGO:00650 RGO:00651 displacement of small bowel loops RGO:00651 SNOMEDCT:3558002 RGO:00664 mesenteric infarction RGO:00664 RADLEX:RID4588 SNOMEDCT:73817000 RGO:00666 radiation enteritis RGO:00666 RGO:00674 endometrial implant RGO:00674 RGO:00677 inverted Meckel diverticulum RGO:00677 adenomas DOID:657 RADLEX:RID4211 SNOMEDCT:32048006 SNOMEDCT:443416007 RGO:00683 adenoma RGO:00683 fibrous hamartoma DOID:0050871 HP:0010614 RADLEX:RID4289 SNOMEDCT:112682009 SNOMEDCT:424568000 RGO:00684 fibroma RGO:00684 DOID:299 RADLEX:RID4226 SNOMEDCT:35917007 SNOMEDCT:443961001 RGO:00689 adenocarcinoma RGO:00689 RGO:00705 small bowel diverticulum RGO:00705 RGO:00706 duodenal diverticulum RGO:00706 RGO:00708 giant duodenal diverticulum RGO:00708 RGO:00709 jejunal diverticulum RGO:00709 RADLEX:RID4818 RGO:00710 ileal diverticulum RGO:00710 DOID:9487 HP:0002245 RADLEX:RID4818 SNOMEDCT:127962001 SNOMEDCT:37373007 RGO:00711 Meckel diverticulum RGO:00711 RGO:00712 small bowel pseudodiverticulum RGO:00712 RGO:00715 communicating ileal duplication RGO:00715 RGO:00717 intraluminal duodenal diverticulum RGO:00717 RGO:00732 A-beta-lipoproteinemia RGO:00732 RGO:00736 interloop abscess RGO:00736 DOID:4989 HP:0001733 RADLEX:RID3529 SNOMEDCT:75694006 RGO:00739 pancreatitis RGO:00739 lymphoplasmacytic lymphoma HP:0005508 ORDO:33226 SNOMEDCT:35562000 RGO:00742 Waldenström macroglobulinemia RGO:00742 DOID:3345 HP:0000991 SNOMEDCT:63103006 RGO:00743 xanthomatosis RGO:00743 RGO:00750 potassium enteritis RGO:00750 angioedema DOID:1558 ICD10CM:T78.3 SNOMEDCT:41291007 RGO:00755 angioneurotic edema RGO:00755 RGO:00763 radiation enteropathy RGO:00763 RGO:00771 fold thickening of stomach and small bowel RGO:00771 RGO:00773 gastric varices with hypoproteinemia RGO:00773 blind pouch syndrome stagnant loop syndrome stagnant small bowel syndrome DOID:10606 RADLEX:RID4600 SNOMEDCT:77225009 RGO:00777 blind loop syndrome RGO:00777 DOID:0050605 ICD10CM:E83.2 SNOMEDCT:37702000 RGO:00783 acrodermatitis enteropathica RGO:00783 RGO:00784 acute bacterial infection RGO:00784 acquired immunodeficiency syndrome DOID:635 RADLEX:RID34730 SNOMEDCT:62479008 RGO:00785 AIDS RGO:00785 RGO:00787 bile duct obstruction RGO:00787 RADLEX:RID4843 SNOMEDCT:118622000 SNOMEDCT:428794004 RGO:00794 fistula RGO:00794 HSP Henoch-Schönlein syndrome Schönlein-Henoch syndrome allergic vasculitis anaphylactoid purpura leukocytoclastic vasculitis rheumatoid purpura DOID:11123 SNOMEDCT:191306005 RGO:00795 Henoch-Schönlein purpura RGO:00795 chronic bowel ischemia RGO:00802 chronic ischemia of intestine RGO:00802 RGO:00803 jejunal diverticulosis RGO:00803 RGO:00805 peritoneal metastasis RGO:00805 DOID:1184 HP:0000100 ICD10CM:N04 SNOMEDCT:52254009 RGO:00807 nephrotic syndrome RGO:00807 DOID:10611 HP:0002243 SNOMEDCT:66972006 RGO:00809 protein-losing enteropathy RGO:00809 SNOMEDCT:197011006 RGO:00810 radiation gastroenteritis RGO:00810 DOID:9801 ICD10CM:A18.31 SNOMEDCT:44572005 RGO:00811 tuberculous peritonitis RGO:00811 RGO:00815 small bowel stricture with proximal dilatation RGO:00815 ICD10CM:Q43.4 SNOMEDCT:3845008 RGO:00817 duplication of intestine RGO:00817 RGO:00820 dilated small bowel with thick mucosal folds RGO:00820 RGO:00823 metastatic disease to bowel wall or mesentery RGO:00823 RGO:00829 dilated small bowel with normal mucosal folds RGO:00829 RGO:00832 mechanical obstruction RGO:00832 HP:0025130 SNOMEDCT:237975008 RGO:00837 lactase deficiency RGO:00837 SNOMEDCT:95549001 RGO:00846 retroperitoneal hemorrhage RGO:00846 SNOMEDCT:206525008 RGO:00859 neonatal necrotizing enterocolitis RGO:00859 HP:0000016 SNOMEDCT:130951007 SNOMEDCT:267064002 RGO:00861 urinary retention RGO:00861 RGO:00862 chronic nonobstructive small bowel distention RGO:00862 RADLEX:RID1639 SNOMEDCT:65310005 RGO:00865 vagotomy RGO:00865 SNOMEDCT:197024006 RGO:00866 allergic enterocolitis RGO:00866 ORDO:2301 SNOMEDCT:93268000 RGO:00868 congenital short intestine RGO:00868 RGO:00869 diabetes with hypokalemia RGO:00869 RADLEX:RID3500 RGO:00874 mesenteritis RGO:00874 RGO:00879 terminal ileum lesion RGO:00879 DOID:8446 HP:0002576 ICD10CM:K56.1 RADLEX:RID4943 SNOMEDCT:35327006 RGO:00881 intussusception RGO:00881 acute diverticulitis DOID:7475 RADLEX:RID3409 SNOMEDCT:18126004 SNOMEDCT:307496006 RGO:00884 diverticulitis RGO:00884 cathartic abuse purgative abuse SNOMEDCT:280982009 RGO:00887 laxative abuse RGO:00887 RGO:00909 bowel rotation abnormality RGO:00909 HP:0002566 RGO:00910 bowel malrotation RGO:00910 RGO:00912 bowel nonrotation RGO:00912 ICD10CM:Q79.2 SNOMEDCT:396347007 RGO:00913 exomphalos RGO:00913 RGO:00914 extroversion of cloaca RGO:00914 RGO:00916 reverse bowel rotation RGO:00916 RGO:00918 abdominal heterotaxy RGO:00918 ORDO:1335 RGO:00921 Cantrell syndrome RGO:00921 dwarfism-onychodysplasia fifth digit syndrome short stature - onychodysplasia. DOID:1925 ORDO:1465 SNOMEDCT:10007009 RGO:00922 Coffin-Siris syndrome RGO:00922 FG syndrome type 1 Opitz-Kaveggia syndrome DOID:14711 ORDO:93932 SNOMEDCT:49984004 RGO:00923 FG syndrome RGO:00923 RGO:00924 mobile cecum syndrome RGO:00924 DOID:9181 ICD10CM:A06 SNOMEDCT:111910009 RGO:00930 amebiasis RGO:00930 DOID:0060181 ICD10CM:K55.9 RADLEX:RID3431 SNOMEDCT:30588004 RGO:00934 ischemic colitis RGO:00934 DOID:0060859 DOID:11092 ICD10CM:A02.0 SNOMEDCT:302231008 RGO:00936 salmonellosis RGO:00936 RGO:00941 normal lymphoid follicles RGO:00941 DOID:1731 ICD10CM:B39 ORDO:390 SNOMEDCT:12962009 RGO:00943 histoplasmosis RGO:00943 RGO:00945 mycobacterial enteritis RGO:00945 UC DOID:8577 HP:0100279 ICD10CM:K51 RADLEX:RID3476 SNOMEDCT:64766004 RGO:00946 ulcerative colitis RGO:00946 ORDO:31828 RGO:00951 digitalis toxicity RGO:00951 RGO:00956 peritoneal band or adhesion RGO:00956 RGO:00958 vascular compression by extrinsic mass RGO:00958 RGO:00960 abdominal or pelvic inflammatory disease RGO:00960 RGO:00964 fibromuscular hyperplasia of mesenteric artery RGO:00964 SNOMEDCT:24803000 SNOMEDCT:81018009 RGO:00967 radiation injury RGO:00967 RGO:00968 transient ischemia of children RGO:00968 RGO:00969 trauma to the intestine or its vessels RGO:00969 DOID:1770 ICD10CM:K59.31 SNOMEDCT:28536002 RGO:00974 toxic megacolon RGO:00974 RGO:00979 diabetes with gas-forming organism RGO:00979 RGO:00981 Hirschsprung disease or other megacolon RGO:00981 DOID:1240 HP:0001909 RADLEX:RID3863 SNOMEDCT:87163000 SNOMEDCT:93143009 RGO:00983 leukemia RGO:00983 RGO:00986 perforated jejunal diverticulum RGO:00986 RGO:00987 pneumomediastinum with abdominal extension of air RGO:00987 RGO:00991 trauma to gut RGO:00991 RGO:00996 infarcted bowel RGO:00996 DOID:865 HP:0002633 RADLEX:RID3681 SNOMEDCT:31996006 RGO:01004 vasculitis RGO:01004 RADLEX:RID4801 SNOMEDCT:87241003 RGO:01006 pneumatosis RGO:01006 RGO:01008 submucosal fat deposition RGO:01008 GIST DOID:9253 HP:0100723 ICD10CM:C49.A ORDO:44890 RADLEX:RID4551 SNOMEDCT:128755003 SNOMEDCT:420120006 RGO:01010 gastrointestinal stromal tumor RGO:01010 RGO:01012 bowel edema in cirrhosis RGO:01012 SNOMEDCT:699223005 RGO:01013 submucosal hemorrhage RGO:01013 RGO:01016 metastatic disease involving bowel wall RGO:01016 CMV infection DOID:11259 SNOMEDCT:28944009 RGO:01017 cytomegalovirus infection RGO:01017 ICD10CM:K56.41 SNOMEDCT:44635007 SNOMEDCT:67409000 RGO:01035 fecal impaction RGO:01035 RGO:01036 gastric obstruction RGO:01036 RGO:01037 nonobstructive ileus RGO:01037 DOID:1733 ICD10CM:A07.2 ORDO:1549 SNOMEDCT:240370009 RGO:01040 cryptosporidiosis RGO:01040 DOID:2074 SNOMEDCT:56905009 RGO:01044 perforation of intestine RGO:01044 SNOMEDCT:56226004 RGO:01046 stricture of intestine RGO:01046 RGO:01047 intestinal obstruction in a newborn RGO:01047 aganglinosis DOID:10487 HP:0002251 ORDO:388 RADLEX:RID5282 SNOMEDCT:204739008 RGO:01050 Hirschsprung disease RGO:01050 RGO:01051 malrotation with midgut volvulus RGO:01051 ICD10CM:P76.0 SNOMEDCT:206528005 RGO:01052 meconium plug syndrome RGO:01052 SNOMEDCT:253782006 RGO:01053 small left colon syndrome RGO:01053 RGO:01054 apple peel intestinal atresia RGO:01054 RGO:01055 inspissated milk syndrome RGO:01055 HP:0100668 RGO:01056 intestinal duplication RGO:01056 RGO:01057 intraluminal diaphragm or web RGO:01057 RGO:01064 segmental dilatation of ileum RGO:01064 RGO:01065 intestinal obstruction in a child RGO:01065 familial recurrent polyserositis DOID:2987 ICD10CM:M04.1 ORDO:342 SNOMEDCT:12579009 RGO:01071 familial Mediterranean fever RGO:01071 ICD10CM:A18.32 SNOMEDCT:12137005 RGO:01078 tuberculous enteritis RGO:01078 RGO:01080 intestinal obstruction in an adult RGO:01080 DOID:289 HP:0030127 ICD10CM:N80 RADLEX:RID3870 SNOMEDCT:129103003 SNOMEDCT:396224008 RGO:01089 endometriosis RGO:01089 ICD10CM:K56.3 RADLEX:RID4965 SNOMEDCT:37976006 RGO:01091 gallstone ileus RGO:01091 fibrosing mesenteritis mesenteric fibrosis DOID:8283 ICD10CM:K65.4 SNOMEDCT:86422009 RGO:01098 retractile mesenteritis RGO:01098 SNOMEDCT:444546002 RGO:01100 chronic ulcerative colitis RGO:01100 RADLEX:RID1705 RGO:01111 jejunoileal bypass RGO:01111 SNOMEDCT:95625008 RGO:01112 neonatal adynamic ileus RGO:01112 hypovitaminosis D DOID:10574 HP:0100512 ICD10CM:E55 SNOMEDCT:34713006 RGO:01117 vitamin D deficiency RGO:01117 DOID:2326 RADLEX:RID3461 SNOMEDCT:25374005 RGO:01130 gastroenteritis RGO:01130 DOID:8445 HP:0002580 ICD10CM:K56.2 RADLEX:RID4786 SNOMEDCT:9707006 RGO:01131 volvulus RGO:01131 periappendiceal abscess SNOMEDCT:62224002 RGO:01133 appendiceal abscess RGO:01133 RGO:01140 extrinsic mass RGO:01140 RADLEX:RID3955 SNOMEDCT:19633006 RGO:01142 mucocele RGO:01142 RGO:01143 myxoglobulosis RGO:01143 RGO:01154 solitary filling defect in colon RGO:01154 RADLEX:RID5189 RGO:01159 amyloidoma RGO:01159 RADLEX:RID34767 SNOMEDCT:103678008 SNOMEDCT:237116001 RGO:01161 endometrioma RGO:01161 DOID:3720 ICD10CM:C90.2 SNOMEDCT:128921005 SNOMEDCT:188718006 RGO:01162 extramedullary plasmacytoma RGO:01162 RGO:01164 inverted colonic diverticulum RGO:01164 RGO:01166 mucormycoma RGO:01166 ORDO:209964 RADLEX:RID5040 SNOMEDCT:716685003 RGO:01174 solitary rectal ulcer syndrome RGO:01174 SNOMEDCT:15202009 RGO:01175 tuberculoma RGO:01175 colon mass colon tumor colonic mass DOID:235 RGO:01177 colonic tumor RGO:01177 RADLEX:RID4224 SNOMEDCT:61722000 RGO:01180 tubulovillous adenoma RGO:01180 DOID:5524 SNOMEDCT:15176003 RGO:01182 adenoacanthoma RGO:01182 DOID:4830 RADLEX:RID4241 SNOMEDCT:403902008 SNOMEDCT:59367005 RGO:01183 adenosquamous carcinoma RGO:01183 SCC epidermoid carcinoma DOID:1749 HP:0002860 RADLEX:RID4259 SNOMEDCT:28899001 SNOMEDCT:402815007 RGO:01184 squamous cell carcinoma RGO:01184 DOID:4236 RADLEX:RID4528 SNOMEDCT:63264007 RGO:01186 carcinosarcoma RGO:01186 SNOMEDCT:86293007 RGO:01187 adenocarcinoid tumor RGO:01187 RGO:01190 smooth-muscle tumor RGO:01190 RGO:01192 vascular tumor RGO:01192 DOID:3462 HP:0010566 RADLEX:RID4335 SNOMEDCT:400006008 SNOMEDCT:51398009 RGO:01193 hamartoma RGO:01193 ORDO:2929 RGO:01195 juvenile polyposis RGO:01195 RADLEX:RID3427 SNOMEDCT:40663003 RGO:01197 colitis cystica profunda RGO:01197 SNOMEDCT:80297003 RGO:01198 lymphoid polyp RGO:01198 SNOMEDCT:76235005 RGO:01199 inflammatory polyp RGO:01199 SNOMEDCT:20958005 RGO:01201 ameboma RGO:01201 RGO:01205 helminthoma RGO:01205 ICD10CM:K66.0 RGO:01212 adhesive bands RGO:01212 RGO:01216 foreign body perforation with pericolic abscess RGO:01216 DOID:13819 SNOMEDCT:186946009 RGO:01217 lymphogranuloma venereum RGO:01217 DOID:3927 SNOMEDCT:190802005 RGO:01223 pelvic lipomatosis RGO:01223 RGO:01224 radiation fibrosis RGO:01224 RADLEX:RID3422 SNOMEDCT:61564002 RGO:01227 typhlitis RGO:01227 SNOMEDCT:31113003 SNOMEDCT:397881000 RGO:01232 diverticulosis RGO:01232 RGO:01236 amebomas RGO:01236 BRRS Bannayan syndrome Bannayan-Zonana syndrome Riley-Smith syndrome Ruvalcaba-Myhre-Smith syndrome DOID:0050657 ORDO:109 SNOMEDCT:234138005 RGO:01237 Bannayan-Riley-Ruvalcaba syndrome RGO:01237 ORDO:79665 SNOMEDCT:60876000 RGO:01240 Gardner syndrome RGO:01240 HP:0007461 RADLEX:RID3983 SNOMEDCT:254785001 SNOMEDCT:47669001 RGO:01241 hemangiomatosis RGO:01241 RGO:01243 lipomatous polyposis RGO:01243 RADLEX:RID3488 SNOMEDCT:50707001 RGO:01245 malacoplakia RGO:01245 DOID:13249 SNOMEDCT:17465007 RGO:01251 pneumatosis cystoides intestinalis RGO:01251 SNOMEDCT:61665008 RGO:01254 Turcot syndrome RGO:01254 RGO:01259 Helicobacter fetus colitis RGO:01259 DOID:0060183 ICD10CM:K52.831 ORDO:36205 RADLEX:RID3428 SNOMEDCT:19311003 RGO:01263 collagenous colitis RGO:01263 ORDO:330021 SNOMEDCT:85180002 RGO:01268 mercury poisoning RGO:01268 RGO:01270 nonspecific benign ulceration of colon RGO:01270 SNOMEDCT:55809007 RGO:01276 radiation colitis RGO:01276 RGO:01277 Salmonella colitis RGO:01277 SNOMEDCT:197178009 RGO:01284 pericolic abscess RGO:01284 SNOMEDCT:76570008 RGO:01288 foreign body perforation RGO:01288 RGO:01291 renal infection or abscess RGO:01291 RGO:01292 double tracking of barium in the distal colon RGO:01292 DOID:1520 SNOMEDCT:269533000 RGO:01293 carcinoma of colon RGO:01293 RGO:01294 smooth colon RGO:01294 RGO:01304 colonic distention without obstruction RGO:01304 RGO:01311 ureteral colic RGO:01311 SNOMEDCT:30693006 RGO:01312 aerophagia RGO:01312 RGO:01319 idiopathic intestinal pseudo-obstruction RGO:01319 DOID:11372 HP:0002251 SNOMEDCT:33995003 RGO:01325 megacolon RGO:01325 RADLEX:RID34705 SNOMEDCT:89049001 RGO:01333 duplication RGO:01333 ORDO:294 RGO:01334 fetal cytomegalovirus infection RGO:01334 MEN MEN syndrome multiple endocrine neoplasia DOID:3125 RGO:01336 multiple endocrine neoplasia syndrome RGO:01336 DOID:1498 ICD10CM:A00 ORDO:173 SNOMEDCT:63650001 RGO:01347 cholera RGO:01347 DOID:10955 ICD10CM:B78 ORDO:76 SNOMEDCT:1214006 RGO:01349 strongyloidiasis RGO:01349 RGO:01358 microcolon of prematurity RGO:01358 RGO:01363 cecal lesion RGO:01363 fecalith RADLEX:RID4985 SNOMEDCT:197063004 RGO:01373 enterolith RGO:01373 RGO:01374 ileus of cecum RGO:01374 DOID:7033 ICD10CM:B81.0 ORDO:1070 SNOMEDCT:442652006 RGO:01392 anisakiasis RGO:01392 RGO:01395 ileocolic prolapse RGO:01395 RADLEX:RID3780 SNOMEDCT:128863005 SNOMEDCT:43961000 RGO:01396 lymphoid hyperplasia RGO:01396 SNOMEDCT:195277008 RGO:01403 aneurysm of internal iliac artery RGO:01403 SNOMEDCT:117169008 RGO:01405 hydatid cyst RGO:01405 DOID:4347 RADLEX:RID4892 SNOMEDCT:234109007 RGO:01406 lymphocele RGO:01406 RGO:01408 sling repair for rectal prolapse RGO:01408 RADLEX:RID4879 RGO:01410 urinoma RGO:01410 RADLEX:RID4787 SNOMEDCT:29696001 RGO:01416 prolapse RGO:01416 ICD10CM:K62.7 ORDO:70475 SNOMEDCT:235760009 RGO:01417 radiation proctitis RGO:01417 HP:0000143 ICD10CM:N82.3 RADLEX:RID4846 SNOMEDCT:65619001 RGO:01424 rectovaginal fistula RGO:01424 DOID:1395 ORDO:1247 SNOMEDCT:10087007 RGO:01430 schistosomiasis RGO:01430 adenopathy HP:0002716 RADLEX:RID3798 SNOMEDCT:30746006 RGO:01436 lymphadenopathy RGO:01436 RGO:01442 amyloidosis of colon RGO:01442 HP:0007293 RGO:01443 anterior sacral meningocele RGO:01443 RGO:01446 hemorrhoidal injection RGO:01446 RGO:01448 inguinal hernia with rectal traction RGO:01448 SNOMEDCT:122449004 RGO:01451 pneumoretroperitoneum RGO:01451 intramural hematoma of intestinal tract intramural hemorrhage of intestinal tract RGO:01463 intramural gastrointestinal tract hemorrhage RGO:01463 ITP autoimmune thrombocytopenic purpura immune thrombocytopenia primary immune thrombocytopenia primary immune thrombocytopenic purpura DOID:8924 HP:0001973 ICD10CM:D69.3 ORDO:3002 SNOMEDCT:32273002 RGO:01468 idiopathic thrombocytopenic purpura RGO:01468 DOID:4358 RGO:01471 metastatic melanoma RGO:01471 DOID:6755 SNOMEDCT:37279009 RGO:01472 amyloid tumor RGO:01472 ICD10CM:C96.6 ICD10CM:K13.4 ORDO:99871 RADLEX:RID3849 SNOMEDCT:128810002 SNOMEDCT:129000002 RGO:01473 eosinophilic granuloma RGO:01473 Bean syndrome ORDO:1059 SNOMEDCT:254784002 RGO:01476 blue rubber bleb nevus syndrome RGO:01476 RGO:01486 biliary-enteric fistula RGO:01486 RGO:01489 entero-ovarian fistula RGO:01489 RGO:01494 prosthetic aortic graft RGO:01494 RADLEX:RID1670 SNOMEDCT:38102005 RGO:01500 cholecystectomy RGO:01500 DOID:13608 HP:0005912 ORDO:30391 SNOMEDCT:77480004 RGO:01503 biliary atresia RGO:01503 RGO:01505 compression by adjacent mass RGO:01505 RGO:01507 fibrosis of gallbladder RGO:01507 RGO:01510 metastatic disease involving gallbladder RGO:01510 DOID:2237 HP:0200119 SNOMEDCT:37871000 RGO:01514 acute hepatitis RGO:01514 DOID:1949 ICD10CM:K81.1 SNOMEDCT:20824003 RGO:01515 chronic cholecystitis RGO:01515 RGO:01517 adenomyomatosis of gallbladder RGO:01517 RGO:01520 obstructing gallstone RGO:01520 RGO:01528 prolonged fasting RGO:01528 hypersomatotropism DOID:2449 HP:0000845 ORDO:963 RADLEX:RID34836 RADLEX:RID46043 SNOMEDCT:74107003 RGO:01529 acromegaly RGO:01529 DOID:2297 ICD10CM:A27 ORDO:509 SNOMEDCT:77377001 RGO:01533 leptospirosis RGO:01533 TPN hyperalimentation SNOMEDCT:225372007 RGO:01535 total parenteral nutrition RGO:01535 RGO:01536 gallstone in cystic duct RGO:01536 scarlatina DOID:8596 ICD10CM:A38 SNOMEDCT:30242009 RGO:01537 scarlet fever RGO:01537 SNOMEDCT:54150009 RGO:01538 upper respiratory infection RGO:01538 RADLEX:RID3869 SNOMEDCT:699661003 RGO:01540 adenomyomatosis RGO:01540 strawberry gallbladder RADLEX:RID5215 SNOMEDCT:48319001 RGO:01541 cholesterolosis RGO:01541 RADLEX:RID28795 SNOMEDCT:276654001 RGO:01542 congenital malformation RGO:01542 RGO:01543 desquamated gallbladder mucosa RGO:01543 RGO:01545 cystic duct obstruction RGO:01545 RADLEX:RID5199 RGO:01547 milk of calcium bile RGO:01547 DOID:9765 RADLEX:RID3396 SNOMEDCT:95558008 RGO:01550 emphysematous cholecystitis RGO:01550 RGO:01551 ruptured gallbladder RGO:01551 RGO:01552 calcification in gallbladder or common bile duct RGO:01552 RGO:01555 mucinous adenocarcinoma of gallbladder RGO:01555 calcified gallbladder calcified gallbladder wall RADLEX:RID5198 SNOMEDCT:110995008 RGO:01556 porcelain gallbladder RGO:01556 RADLEX:RID3885 SNOMEDCT:46983009 RGO:01560 cholesterol polyp RGO:01560 SNOMEDCT:46341007 RGO:01565 cholecystitis glandularis proliferans RGO:01565 RGO:01574 postoperative defect RGO:01574 DOID:9766 RADLEX:RID3709 SNOMEDCT:448286002 RGO:01577 xanthogranulomatous cholecystitis RGO:01577 RGO:01582 desquamated mucosa RGO:01582 RGO:01583 fibrinous debris RGO:01583 RGO:01584 inspissated pus RGO:01584 RGO:01586 precipitated contrast medium from ERCP RGO:01586 DOID:1949 ICD10CM:K81.0 SNOMEDCT:65275009 RGO:01588 acute cholecystitis RGO:01588 RADLEX:RID3887 SNOMEDCT:82375006 RGO:01589 adenomatous polyp RGO:01589 RADLEX:RID4994 SNOMEDCT:56381008 RGO:01590 calculus RGO:01590 RGO:01591 fold in gallbladder wall RGO:01591 RGO:01592 AIDS-related cholangiopathy RGO:01592 ICD10CM:K81.0 SNOMEDCT:73125001 RGO:01595 empyema of gallbladder RGO:01595 SNOMEDCT:419603000 RGO:01596 epithelial cyst RGO:01596 RGO:01598 food particles after cholecystojejunostomy RGO:01598 ICD10CM:K81.0 RADLEX:RID3397 RGO:01599 gangrenous cholecystitis RGO:01599 HP:0100762 SNOMEDCT:66556007 RGO:01600 hemobilia RGO:01600 RGO:01601 hemorrhagic cholecystitis RGO:01601 RADLEX:RID5197 RGO:01602 milk of calcium RGO:01602 RGO:01604 sarcoma of gallbladder RGO:01604 RGO:01608 extrahepatic biliary obstruction RGO:01608 SNOMEDCT:260882000 SNOMEDCT:404227002 SNOMEDCT:73320003 RGO:01609 hemolysis RGO:01609 RGO:01615 administration of parenteral nutrition and furosemide to premature infant RGO:01615 RGO:01616 biliary tree malformation RGO:01616 DOID:13580 HP:0001396 SNOMEDCT:33688009 RGO:01617 cholestasis RGO:01617 HP:0001472 RGO:01618 familial predisposition RGO:01618 RGO:01620 hepatic dysfunction RGO:01620 RGO:01621 methadone intake RGO:01621 RGO:01622 monochorionic twin after intrauterine death of its co-twin RGO:01622 HP:0100806 RADLEX:RID39263 SNOMEDCT:91302008 RGO:01623 sepsis RGO:01623 RGO:01627 empyema of gallbladder with pus RGO:01627 RGO:01631 vicarious excretion of contrast medium RGO:01631 RGO:01632 volume averaging with adjacent structures RGO:01632 SNOMEDCT:48033007 RGO:01637 microabscess RGO:01637 SNOMEDCT:22149007 RGO:01638 Rokitansky-Aschoff sinuses RGO:01638 RGO:01643 ectopic mucosa RGO:01643 portal venous hypertension DOID:10762 HP:0001409 ICD10CM:K76.6 RADLEX:RID34614 SNOMEDCT:34742003 RGO:01651 portal hypertension RGO:01651 DOID:11077 ICD10CM:A23 ORDO:1304 SNOMEDCT:75702008 RGO:01654 brucellosis RGO:01654 RGO:01656 folds in gallbladder wall RGO:01656 RGO:01657 gangrenous gallbladder RGO:01657 DOID:8568 ICD10CM:B27 SNOMEDCT:271558008 RGO:01658 infectious mononucleosis RGO:01658 RGO:01660 lymphatic obstruction at porta hepatis RGO:01660 myeloma DOID:9538 HP:0006775 ICD10CM:C90.0 ORDO:29073 RADLEX:RID3864 SNOMEDCT:109989006 SNOMEDCT:55921005 RGO:01661 multiple myeloma RGO:01661 RGO:01662 necrotizing enterocolitis in infants RGO:01662 RGO:01663 peptic ulcer adjacent to gallbladder RGO:01663 RGO:01664 pyelonephritis of right kidney RGO:01664 DOID:14268 HP:0030991 ICD10CM:K83.0 SNOMEDCT:235917005 RGO:01665 sclerosing cholangitis RGO:01665 RGO:01671 blockage of lymphatic and venous drainage of gallbladder RGO:01671 DOID:2237 HP:0012115 RADLEX:RID3467 SNOMEDCT:128241005 RGO:01672 hepatitis RGO:01672 inflammation of peritoneal cavity DOID:8283 HP:0002586 ICD10CM:K65 RADLEX:RID3535 SNOMEDCT:48661000 RGO:01683 peritonitis RGO:01683 RGO:01684 delayed scintigraphic visualization of gallbladder RGO:01684 RGO:01685 acalculus cholecystitis RGO:01685 black liver-jaundice syndrome hyperbilirubinemia II icterus-hepatic pigmentation syndrome DOID:12308 ICD10CM:E80.6 ORDO:234 SNOMEDCT:44553005 RGO:01686 Dubin-Johnson syndrome RGO:01686 RGO:01690 cholecystitis with perforation RGO:01690 RGO:01695 common duct entry into duodenal diverticulum RGO:01695 RGO:01699 peptic ulcer with perforation into common duct and fistula RGO:01699 DOID:0050876 ORDO:53035 RADLEX:RID34711 SNOMEDCT:717232005 RGO:01705 Caroli disease RGO:01705 inspissated bile syndrome RGO:01708 bile plug syndrome RGO:01708 SNOMEDCT:49808004 RGO:01713 advanced age RGO:01713 RADLEX:RID3896 SNOMEDCT:397868007 RGO:01725 choledochocele RGO:01725 SNOMEDCT:4283007 RGO:01730 Mirizzi syndrome RGO:01730 RGO:01731 periportal edema RGO:01731 RGO:01732 biliary dilatation without jaundice or obstruction RGO:01732 RGO:01734 common duct exploration sequela RGO:01734 RGO:01735 early biliary ductal obstruction RGO:01735 RGO:01736 nonobstructive gallstone RGO:01736 RGO:01739 post-ductal obstruction RGO:01739 RGO:01740 recent passage of stone with ampullary edema RGO:01740 RGO:01741 biliary obstruction without dilatation RGO:01741 DOID:4947 HP:0030153 ICD10CM:C22.1 ORDO:70567 RADLEX:RID4266 SNOMEDCT:70179006 RGO:01743 cholangiocarcinoma RGO:01743 RGO:01746 cystic and saccular lesions of bile ducts with normal-sized intrahepatic bile ducts RGO:01746 RGO:01747 biliary cystadenoma RGO:01747 RGO:01750 cystic duct remnant RGO:01750 RGO:01752 simple central dilatation of common duct RGO:01752 RGO:01753 cystic and saccular lesions of bile ducts with dilatation of intrahepatic bile ducts RGO:01753 RGO:01757 reversible dilatation of intrahepatic bile ducts RGO:01757 SNOMEDCT:56117007 RGO:01760 air bubble RGO:01760 RGO:01774 pericholedochal adhesions RGO:01774 ICD10CM:K83.4 SNOMEDCT:28132005 RGO:01777 spasm of sphincter of Oddi RGO:01777 bile duct calculus bile duct stone calculus in biliary duct DOID:11755 RADLEX:RID4992 RGO:01780 choledocholithiasis RGO:01780 air in biliary tree RGO:01785 pneumobilia RGO:01785 RADLEX:RID1555 SNOMEDCT:11311000 SNOMEDCT:367646009 RGO:01786 pus RGO:01786 RADLEX:RID5607 SNOMEDCT:386010000 RGO:01791 surgical clip RGO:01791 DOID:9446 HP:0030151 ICD10CM:K83.0 RADLEX:RID3384 SNOMEDCT:82403002 RGO:01794 cholangitis RGO:01794 RGO:01801 artifact from post-processing technique of MRCP RGO:01801 RGO:01802 biliary hypoplasia or atresia RGO:01802 RGO:01810 papillitis of ampulla RGO:01810 RGO:01812 postbulbar duodenal ulcer with scarring or perforation RGO:01812 RGO:01816 enlarged papilla of vater RGO:01816 RGO:01817 calculus impacted in distal common duct RGO:01817 RGO:01818 carcinoma of Vaterian segment RGO:01818 DOID:10175 SNOMEDCT:73221001 RGO:01821 papillitis RGO:01821 RGO:01822 edema secondary to active duodenal ulcer RGO:01822 RGO:01823 heterotopic pancreatic tissue RGO:01823 RGO:01833 diverticulitis of duodenum or hepatic flexure of colon RGO:01833 RGO:01836 passage of common duct stone RGO:01836 RGO:01837 peptic ulcer perforation into biliary tract RGO:01837 RGO:01841 biliary obstruction RGO:01841 HP:0002240 RADLEX:RID34593 SNOMEDCT:80515008 RGO:01845 hepatomegaly RGO:01845 ICD10CM:Q44.7 SNOMEDCT:407000 RGO:01848 congenital hepatomegaly RGO:01848 HP:0001978 RADLEX:RID3838 SNOMEDCT:42952007 RGO:01858 extramedullary hematopoiesis RGO:01858 kala-azar DOID:9065 ICD10CM:B55 ORDO:507 SNOMEDCT:80612004 RGO:01863 leishmaniasis RGO:01863 PC PCV erythremia polycythaemia vera polycythemia rubra vera primary polycythemia DOID:8997 ICD10CM:D45 ORDO:729 RADLEX:RID3865 SNOMEDCT:109992005 SNOMEDCT:128841001 RGO:01866 polycythemia vera RGO:01866 DOID:14525 SNOMEDCT:74351001 RGO:01867 Reye syndrome RGO:01867 DOID:11335 ICD10CM:D86 ORDO:797 RADLEX:RID34662 SNOMEDCT:31541009 RGO:01868 sarcoidosis RGO:01868 Aase-Smith syndrome II SNOMEDCT:71988008 RGO:01876 Aase syndrome RGO:01876 Chiari syndrome hepatic outflow obstruction hepatic vein thrombosis hepatic venous thrombosis thrombosis of hepatic veins DOID:11512 HP:0002639 ICD10CM:I82.0 ORDO:131 RADLEX:RID46044 SNOMEDCT:82385007 RGO:01880 Budd-Chiari syndrome RGO:01880 DOID:14502 ORDO:75234 SNOMEDCT:57218003 RGO:01882 cholesterol ester storage disease RGO:01882 DOID:1064 ICD10CM:E72.04 ORDO:213 SNOMEDCT:190681003 RGO:01885 cystinosis RGO:01885 SNOMEDCT:64235006 RGO:01886 ethanolaminosis RGO:01886 DOID:11042 ORDO:47612 SNOMEDCT:57160007 RGO:01888 Felty syndrome RGO:01888 DOID:9870 HP:0012024 ICD10CM:E74.21 ORDO:352 ORDO:79239 SNOMEDCT:190745006 RGO:01889 galactosemia RGO:01889 HP:0010980 SNOMEDCT:3744001 RGO:01893 hyperlipoproteinemia RGO:01893 SNOMEDCT:80660001 RGO:01895 Mauriac syndrome RGO:01895 SNOMEDCT:124331002 RGO:01898 pyruvate kinase deficiency RGO:01898 sea-blue histiocytosis DOID:4423 SNOMEDCT:37821003 RGO:01899 sea-blue histiocyte syndrome RGO:01899 RGO:01916 fetal or neonatal liver calcification RGO:01916 DOID:4173 SNOMEDCT:704152002 RGO:01918 metastatic neuroblastoma RGO:01918 RGO:01927 carbon tetrachloride exposure RGO:01927 RGO:01931 hepatotoxin RGO:01931 DOID:8477 SNOMEDCT:32230006 RGO:01933 malabsorption syndrome RGO:01933 SNOMEDCT:71192002 RGO:01934 peritoneal dialysis RGO:01934 RGO:01939 cirrhosis with arterial-portal shunt RGO:01939 RGO:01940 hypervascular gallbladder disease RGO:01940 RGO:01944 ethanol ablation RGO:01944 RGO:01945 obstruction of peripheral portal branches RGO:01945 SNOMEDCT:274314005 RGO:01946 percutaneous needle biopsy RGO:01946 SNOMEDCT:445925008 RGO:01952 lymphomatous infiltration RGO:01952 DOID:7997 SNOMEDCT:90739004 RGO:01953 thyrotoxicosis RGO:01953 DOID:0080169 HP:0011662 ORDO:1209 SNOMEDCT:63042009 RGO:01954 tricuspid atresia RGO:01954 RGO:01957 malignant infiltration of liver by primary or metastatic neoplasm RGO:01957 DOID:9861 ICD10CM:A19 SNOMEDCT:47604008 RGO:01971 miliary tuberculosis RGO:01971 DOID:9275 HP:0003231 ICD10CM:E70.21 SNOMEDCT:190694001 RGO:01972 tyrosinemia RGO:01972 DOID:12119 RADLEX:RID5203 SNOMEDCT:39011001 RGO:01974 hemosiderosis RGO:01974 RGO:01975 chronic arsenic poisoning RGO:01975 RGO:01980 Thorotrast RGO:01980 RGO:01990 calcified granulomas RGO:01990 RGO:01992 Gamna-Gandy bodies RGO:01992 RGO:01997 periportal vascular collaterals RGO:01997 RGO:01999 superparamagnetic contrast medium RGO:01999 RGO:02000 spontaneous liver rupture RGO:02000 RGO:02002 oral contraceptive use RGO:02002 peliosis hepatitis DOID:914 ICD10CM:K76.4 SNOMEDCT:58008004 RGO:02004 peliosis hepatis RGO:02004 HP:0100603 SNOMEDCT:15394000 RGO:02005 toxemia of pregnancy RGO:02005 SNOMEDCT:91285009 RGO:02014 adrenal rest RGO:02014 SNOMEDCT:39471001 RGO:02016 cholangioma RGO:02016 ORDO:157791 RADLEX:RID3991 SNOMEDCT:403981003 SNOMEDCT:54124005 RGO:02017 epithelioid hemangioendothelioma RGO:02017 fibrolamellar HCC DOID:5015 RADLEX:RID4273 SNOMEDCT:253018005 RGO:02018 fibrolamellar hepatocellular carcinoma RGO:02018 DOID:687 HP:0002884 ICD10CM:C22.2 ORDO:449 RADLEX:RID4530 SNOMEDCT:109843000 SNOMEDCT:45024009 RGO:02022 hepatoblastoma RGO:02022 DOID:3307 HP:0009792 RADLEX:RID4321 SNOMEDCT:55818009 RGO:02027 teratoma RGO:02027 SNOMEDCT:25878000 RGO:02036 aneurysm of hepatic artery RGO:02036 RGO:02037 angiomyolipoma of liver RGO:02037 hepatic angiosarcoma DOID:268 ICD10CM:C22.3 SNOMEDCT:109844006 RGO:02038 angiosarcoma of liver RGO:02038 RGO:02045 visceral larval migrans granuloma RGO:02045 FNH RADLEX:RID3778 SNOMEDCT:22995004 RGO:02050 focal nodular hyperplasia RGO:02050 DOID:3467 RADLEX:RID4340 SNOMEDCT:80656004 RGO:02055 mesenchymal hamartoma RGO:02055 microbiliary hamartoma von Meyenburg complex RGO:02056 multiple bile duct hamartoma RGO:02056 DOID:3305 SNOMEDCT:67830002 RGO:02058 teratocarcinoma RGO:02058 SNOMEDCT:448997008 RGO:02074 hepatic cystadenoma RGO:02074 RGO:02086 biloma RGO:02086 bartonellosis cat scratch fever DOID:11258 ICD10CM:A28.1 ORDO:50839 RGO:02087 cat-scratch disease RGO:02087 RGO:02088 cystic duct remnant with mucocele RGO:02088 ICD10CM:Q44.1 SNOMEDCT:78372005 RGO:02091 intrahepatic gallbladder RGO:02091 VHL von Hippel-Lindau syndrome DOID:14175 ORDO:892 RGO:02095 von Hippel-Lindau disease RGO:02095 HCC hepatoma DOID:684 HP:0001402 ICD10CM:C22.0 ORDO:88673 RADLEX:RID4271 SNOMEDCT:109841003 SNOMEDCT:25370001 RGO:02104 hepatocellular carcinoma RGO:02104 DOID:4075 RGO:02116 biliary cystadenocarcinoma RGO:02116 RADLEX:RID4353 SNOMEDCT:20810002 RGO:02128 myelolipoma RGO:02128 RGO:02129 bulls-eye liver lesion RGO:02129 RGO:02131 septic emboli RGO:02131 DOID:1967 HP:0100243 ORDO:64720 RADLEX:RID4387 SNOMEDCT:443719001 SNOMEDCT:51549004 RGO:02138 leiomyosarcoma RGO:02138 ORDO:48372 RADLEX:RID3790 SNOMEDCT:715141007 RGO:02148 nodular regenerative hyperplasia RGO:02148 DOID:769 HP:0003006 ORDO:635 RADLEX:RID4454 SNOMEDCT:432328008 SNOMEDCT:87364003 RGO:02158 neuroblastoma RGO:02158 RGO:02159 papillary serous cystadenocarcinoma of ovary RGO:02159 ICD10CM:C45 ORDO:50251 RADLEX:RID4377 SNOMEDCT:62064005 RGO:02163 mesothelioma RGO:02163 chorioblastoma chorioepithelioma chorionic carcinoma DOID:3594 HP:0100768 RADLEX:RID4324 SNOMEDCT:188188009 SNOMEDCT:44769000 RGO:02167 choriocarcinoma RGO:02167 SNOMEDCT:314191009 RGO:02169 cystadenocarcinoma of ovary RGO:02169 DOID:3606 RGO:02175 mucinous carcinoma of ovary RGO:02175 DOID:2871 HP:0012114 RGO:02178 endometrial carcinoma of uterus RGO:02178 DOID:3910 SNOMEDCT:254626006 RGO:02182 adenocarcinoma of lung RGO:02182 DOID:1993 SNOMEDCT:254582000 RGO:02185 carcinoma of rectum RGO:02185 DOID:5651 SNOMEDCT:58248003 RGO:02187 anaplastic carcinoma RGO:02187 DOID:2893 SNOMEDCT:285432005 RGO:02188 carcinoma of cervix RGO:02188 RGO:02190 hyperechoic liver metastasis with acoustic shadowing RGO:02190 RGO:02191 mucinous or colloid carcinoma of colon or breast RGO:02191 SNOMEDCT:408647009 RGO:02193 adenocarcinoma of stomach RGO:02193 SNOMEDCT:235966007 RGO:02194 cystadenocarcinoma of pancreas RGO:02194 RGO:02219 congenital simple cyst RGO:02219 SNOMEDCT:55294001 RGO:02231 focal hepatic necrosis RGO:02231 SNOMEDCT:427744002 RGO:02234 hemangioendothelioma of liver RGO:02234 RGO:02238 regenerating liver nodules RGO:02238 RGO:02243 dysplastic liver nodule RGO:02243 RADLEX:RID31756 RGO:02245 hepatic fissure RGO:02245 RGO:02248 omentum inserted into bed of hepatic resection RGO:02248 RGO:02250 solitary fibrous tumor of liver RGO:02250 RGO:02252 sonographically complex hepatic mass RGO:02252 DOID:483 HP:0001048 RADLEX:RID3973 SNOMEDCT:33377007 SNOMEDCT:416824008 RGO:02253 cavernous hemangioma RGO:02253 RGO:02269 linear or branching acoustic shadowing in liver RGO:02269 RGO:02270 air in biliary tract RGO:02270 RGO:02271 air in portal vein RGO:02271 RGO:02272 calculi in biliary ducts RGO:02272 RGO:02274 focal acoustic shadowing in liver RGO:02274 RGO:02297 focal high-attenuation liver lesion RGO:02297 RGO:02302 hepatocellular adenoma with acute hemorrhage RGO:02302 SNOMEDCT:85057007 RGO:02317 hepatic cyst RGO:02317 RGO:02324 proteinaceous material in dependent portion of abscess or hematoma RGO:02324 RGO:02327 extrinsic compression of hepatic veins RGO:02327 RGO:02328 passive hepatic congestion RGO:02328 RGO:02330 hepatic vein dilatation RGO:02330 DOID:11481 HP:0002563 RADLEX:RID28796 SNOMEDCT:85598007 RGO:02331 constrictive pericarditis RGO:02331 RGO:02332 inferior vena cava obstruction or thrombus RGO:02332 RGO:02333 normal with Valsalva maneuver in young patient RGO:02333 HP:0001708 RGO:02334 right-sided heart failure RGO:02334 RGO:02335 thrombus in hepatic vein RGO:02335 RGO:02336 tricuspid atresia or stenosis RGO:02336 RGO:02337 right atrial tumor RGO:02337 DOID:3875 HP:0004418 RADLEX:RID3700 SNOMEDCT:64156001 RGO:02340 thrombophlebitis RGO:02340 RGO:02345 intravenous web RGO:02345 SNOMEDCT:86569001 RGO:02364 postpartum state RGO:02364 SNOMEDCT:14534009 RGO:02369 splenic vein thrombosis RGO:02369 congestive splenomegaly SNOMEDCT:19058002 RGO:02371 Banti syndrome RGO:02371 RGO:02372 cavernous transformation of portal vein RGO:02372 RGO:02376 increased portal vein flow RGO:02376 RGO:02377 retroperitoneal inflammatory disease RGO:02377 RGO:02384 mesenteric ischemia or occlusion and bowel infarction RGO:02384 SNOMEDCT:387666006 RGO:02386 acute gastric dilatation RGO:02386 RGO:02387 necrotic colon carcinoma RGO:02387 RGO:02388 corrosive ingestion causing gastritis RGO:02388 RGO:02389 diabetic acidosis or coma RGO:02389 DOID:1098 SNOMEDCT:387705004 RGO:02390 erythroblastosis fetalis RGO:02390 SNOMEDCT:7399006 RGO:02391 gastric emphysema RGO:02391 SNOMEDCT:4399003 RGO:02392 hemorrhagic pancreatitis RGO:02392 RGO:02393 neonatal gastroenteritis RGO:02393 RGO:02394 peptic ulcer eroding into mesenteric vein RGO:02394 RGO:02399 congestive hepatomegaly RGO:02399 RGO:02402 Schistosomiasis mansoni RGO:02402 DOID:1884 HP:0006562 SNOMEDCT:3738000 RGO:02404 viral hepatitis RGO:02404 DOID:14115 ICD10CM:A48.3 ORDO:36234 SNOMEDCT:18504008 RGO:02414 toxic shock syndrome RGO:02414 RGO:02415 prominent periportal echoes in a neonate RGO:02415 RGO:02417 idiopathic neonatal jaundice RGO:02417 DOID:13603 RADLEX:RID34740 SNOMEDCT:59848001 RGO:02421 obstructive jaundice RGO:02421 SNOMEDCT:34093004 RGO:02423 blood dyscrasia RGO:02423 DOID:11702 HP:0002961 SNOMEDCT:123782009 RGO:02425 dysgammaglobulinemia RGO:02425 DOID:2747 ICD10CM:E74.0 SNOMEDCT:29633007 RGO:02445 glycogen storage disease RGO:02445 RGO:02449 hemorrhagic pseudocyst RGO:02449 HP:0012223 RGO:02450 ruptured spleen RGO:02450 RGO:02452 congenital syndromes RGO:02452 RADLEX:RID11103 SNOMEDCT:302497006 RGO:02454 hemodialysis RGO:02454 DOID:0060216 ORDO:1467 SNOMEDCT:405810005 RGO:02463 Cogan syndrome RGO:02463 RGO:02466 Vaquez-Osler syndrome RGO:02466 DOID:12971 ICD10CM:D58.0 ORDO:822 SNOMEDCT:55995005 RGO:02469 hereditary spherocytosis RGO:02469 chronic idiopathic myelofibrosis myeloid metaplasia myelosclerosis osteomyelofibrosis primary myelofibrosis DOID:4971 HP:0011974 ICD10CM:D75.81 RADLEX:RID3826 SNOMEDCT:52967002 RGO:02471 myelofibrosis RGO:02471 RADLEX:RID4371 SNOMEDCT:403546006 SNOMEDCT:86970009 RGO:02477 lymphangiomatosis RGO:02477 RGO:02478 multifocal microabscess formation RGO:02478 RGO:02479 Noncaseating granulomatous disease RGO:02479 RGO:02484 small or nonvisualized spleen RGO:02484 RGO:02487 hereditary hypoplasia RGO:02487 SCD sickle cell anemia RADLEX:RID34676 SNOMEDCT:417357006 RGO:02490 sickle cell disease RGO:02490 RADLEX:RID4796 SNOMEDCT:191384005 RGO:02492 wandering spleen RGO:02492 DOID:14006 SNOMEDCT:70405009 RGO:02494 splenic artery aneurysm RGO:02494 splenic artery arteriosclerosis RGO:02495 splenic artery atherosclerosis RGO:02495 RGO:02506 splenic artery calcification RGO:02506 DOID:12722 RGO:02509 liver metastasis RGO:02509 RGO:02512 solitary lesion of spleen RGO:02512 SNOMEDCT:70405009 RGO:02513 aneurysm of splenic artery RGO:02513 cystic hygroma macrocystic lymphatic malformation DOID:3081 SNOMEDCT:40225001 RGO:02520 cystic lymphangioma RGO:02520 DOID:0001816 RADLEX:RID3998 SNOMEDCT:39000009 RGO:02521 hemangiosarcoma RGO:02521 RGO:02523 splenic peliosis RGO:02523 RGO:02525 splenic sequestration crisis RGO:02525 RGO:02531 abscess with gas bubbles RGO:02531 RGO:02532 hydatid cyst with hydatid sand RGO:02532 DOID:3721 HP:0011857 ORDO:86855 RADLEX:RID3861 SNOMEDCT:10639003 SNOMEDCT:415112005 RGO:02533 plasmacytoma RGO:02533 RGO:02534 simple cyst with cholesterol crystals RGO:02534 RGO:02547 abnormality on splenic arteriography RGO:02547 RGO:02551 splenic vein abnormality RGO:02551 RGO:02553 avascular mass RGO:02553 RGO:02554 displacement by extrinsic mass RGO:02554 HP:0001907 RADLEX:RID4837 SNOMEDCT:13713005 SNOMEDCT:371039008 RGO:02557 thromboembolism RGO:02557 RGO:02564 retroperitoneal inflammation RGO:02564 RGO:02567 focal pancreatitis RGO:02567 SNOMEDCT:125271003 RGO:02568 thrombosed aneurysm RGO:02568 RGO:02573 pancreaticoblastoma RGO:02573 microcystic adenoma DOID:2631 DOID:5746 RADLEX:RID4169 SNOMEDCT:51608009 RGO:02575 serous cystadenoma RGO:02575 ICD10CM:K86.3 SNOMEDCT:111374002 RGO:02584 pseudocyst of pancreas RGO:02584 DOID:2660 SNOMEDCT:42717009 RGO:02587 cystic teratoma RGO:02587 RGO:02591 liquefaction necrosis of pancreas RGO:02591 SNOMEDCT:700423003 RGO:02600 adenocarcinoma of pancreas RGO:02600 ORDO:676 RADLEX:RID3531 SNOMEDCT:68072000 RGO:02601 hereditary pancreatitis RGO:02601 HP:0001738 SNOMEDCT:37992001 RGO:02603 pancreatic insufficiency RGO:02603 RGO:02604 ruptured pancreas RGO:02604 DOID:0060479 ORDO:811 SNOMEDCT:89454001 RGO:02605 Shwachman-Diamond syndrome RGO:02605 RGO:02609 calculi in pancreatic duct RGO:02609 RGO:02611 gas in pancreatic abscess RGO:02611 RGO:02612 gas in pancreatic pseudocyst communicating with gut RGO:02612 RGO:02614 pancreatic calcification without mass RGO:02614 RGO:02620 hyperparathyroidism with pancreatitis RGO:02620 RGO:02624 Pneumocystis carinii infection RGO:02624 islet cell tumor of pancreas pancreatic islet cell tumor DOID:1799 ICD10CM:D13.7 RADLEX:RID4487 SNOMEDCT:128878003 RGO:02631 islet cell tumor RGO:02631 RGO:02640 fatty pancreatic lesion RGO:02640 RGO:02641 focal fat deposit RGO:02641 SNOMEDCT:248280005 RGO:02644 aging RGO:02644 RGO:02646 lipomatous pseudohypertrophy RGO:02646 DOID:8452 HP:0004395 SNOMEDCT:2492009 RGO:02647 malnutrition RGO:02647 SNOMEDCT:69643006 RGO:02654 abscess of pancreas RGO:02654 angiofollicular lymph node hyperplasia giant lymph node hyperplasia lymphoid hamartoma ICD10CM:D47.Z2 ORDO:160 RADLEX:RID3781 SNOMEDCT:207036003 RGO:02655 Castleman disease RGO:02655 IPMN intraductal papillary mucinous neoplasm RGO:02656 intraductal papillary mucinous tumor of pancreas RGO:02656 RGO:02661 pancreatic mass RGO:02661 RGO:02674 dilated pancreatic duct RGO:02674 RGO:02686 osteophyte of spine RGO:02686 RGO:02691 gas in pancreatic duct RGO:02691 RGO:02692 patulous Vaterian sphincter RGO:02692 RGO:02694 prior Vaterian papillotomy RGO:02694 RGO:02695 duodenal diverticulum communication RGO:02695 SNOMEDCT:86562005 RGO:02701 cystic mesothelioma RGO:02701 echinococcosis DOID:1496 SNOMEDCT:74942003 RGO:02704 hydatid disease RGO:02704 RGO:02706 ovarian cyst or cystic neoplasm RGO:02706 RGO:02707 papillary serous carcinoma of peritoneum RGO:02707 DOID:3559 ORDO:26790 RADLEX:RID4162 SNOMEDCT:112679004 SNOMEDCT:307601000 RGO:02709 pseudomyxoma peritonei RGO:02709 MFH ORDO:2023 SNOMEDCT:34360000 SNOMEDCT:443439001 RGO:02718 malignant fibrous histiocytoma RGO:02718 RGO:02725 mesenteric edema RGO:02725 RGO:02728 peritoneal disease RGO:02728 RGO:02734 cyst of mesentery RGO:02734 RGO:02739 radiation peritonitis RGO:02739 RADLEX:RID4264 SNOMEDCT:307593001 SNOMEDCT:7010000 RGO:02741 carcinomatosis RGO:02741 post-operative state SNOMEDCT:19585003 RGO:02742 postoperative state RGO:02742 DOID:7615 SNOMEDCT:9395006 RGO:02743 sarcomatosis RGO:02743 Nonne-Milroy lymphedema Nonne-Milroy syndrome hereditary lymphedema type 1A primary congenital lymphedema ORDO:79452 RGO:02750 Milroy disease RGO:02750 DOID:1080 ICD10CM:B74 ORDO:2034 SNOMEDCT:105706003 RGO:02753 filariasis RGO:02753 RGO:02756 rupture of abdominal lymphatics RGO:02756 DOID:1754 HP:0001718 SNOMEDCT:79619009 RGO:02762 mitral stenosis RGO:02762 mediastinal lesion SNOMEDCT:94147001 RGO:02767 mediastinal mass RGO:02767 RGO:02772 chronically ill patients RGO:02772 RGO:02773 invasion by neoplastic disease RGO:02773 VOD DOID:0080177 RADLEX:RID3316 RGO:02774 veno-occlusive disease RGO:02774 SNOMEDCT:36746002 RGO:02777 bile peritonitis RGO:02777 DOID:0060329 HP:0031456 ICD10CM:O00 RADLEX:RID4942 SNOMEDCT:34801009 RGO:02778 ectopic pregnancy RGO:02778 RGO:02785 appendiceal perforation RGO:02785 RADLEX:RID4700 SNOMEDCT:131148009 SNOMEDCT:50960005 RGO:02788 hemorrhage RGO:02788 RADLEX:RID5594 SNOMEDCT:257354000 SNOMEDCT:47020004 RGO:02796 ventriculoperitoneal shunt RGO:02796 RGO:02797 antitrypsinase deficiency RGO:02797 RGO:02801 hemolytic anemia with ascites RGO:02801 RGO:02802 hydrometrocolpos with rupture and plastic peritonitis RGO:02802 RGO:02805 metastatic disease to peritoneum RGO:02805 RGO:02817 spontaneous pneumoperitoneum without peritonitis RGO:02817 RGO:02826 pneumoperitoneum with peritonitis RGO:02826 HP:0030717 ICD10CM:P78.0 RADLEX:RID3536 SNOMEDCT:57341009 RGO:02828 meconium peritonitis RGO:02828 RGO:02836 respirator therapy RGO:02836 RGO:02838 gastric rupture of newborn RGO:02838 RGO:02840 perforated peptic or stress ulcer RGO:02840 gas in bowel wall RADLEX:RID4802 RGO:02850 pneumatosis intestinalis RGO:02850 RGO:02851 pneumomediastinum with retroperitoneal extension RGO:02851 gas in portal vein RGO:02852 portal vein gas RGO:02852 RGO:02860 large abdominal gas pocket RGO:02860 distended cecum distention of cecum RGO:02863 cecal distention RGO:02863 RGO:02876 emphysematous peritonitis RGO:02876 RGO:02878 gangrene of liver RGO:02878 RGO:02881 infected ovarian cyst RGO:02881 RGO:02884 diverticultis RGO:02884 RADLEX:RID49916 SNOMEDCT:56021002 SNOMEDCT:715068009 RGO:02905 seroma RGO:02905 DOID:3827 HP:0000776 ICD10CM:Q79.0 ORDO:2140 RADLEX:RID34584 SNOMEDCT:17190001 RGO:02907 congenital diaphragmatic hernia RGO:02907 SNOMEDCT:112798008 RGO:02909 endotracheal intubation RGO:02909 HP:0040187 SNOMEDCT:276669000 RGO:02912 neonatal sepsis RGO:02912 HP:0001944 ICD10CM:E86.0 SNOMEDCT:34095006 RGO:02915 dehydration RGO:02915 RGO:02917 fluid-filled bowel RGO:02917 RGO:02918 large abdominal mass RGO:02918 RGO:02919 midgut volvulus RGO:02919 RGO:02922 decreased abdominal gas in an adult RGO:02922 HP:0002015 ICD10CM:R13.1 RADLEX:RID5266 SNOMEDCT:40739000 RGO:02923 dysphagia RGO:02923 RGO:02926 large abdominal mass displacing bowel laterally RGO:02926 RGO:02937 urinary tract calcification RGO:02937 RGO:02949 hemochromatosis of liver RGO:02949 RGO:02951 ischemic infarct or necrosis of liver RGO:02951 DOID:5875 RGO:02956 retroperitoneal neoplasm RGO:02956 RGO:02958 tuberculous psoas abscess RGO:02958 RGO:02979 nonvisceral abdominal calcification RGO:02979 RADLEX:RID166 SNOMEDCT:73800007 RGO:02993 epiploic appendage RGO:02993 HP:0030010 SNOMEDCT:60023006 RGO:02996 hydrometrocolpos RGO:02996 SNOMEDCT:236002003 RGO:03005 retroperitoneal hematoma RGO:03005 RGO:03010 bladder calculi RGO:03010 RGO:03015 myxoglobulosis of appendix RGO:03015 RGO:03017 urachal cyst calculi RGO:03017 RADLEX:RID1551 RGO:03023 meconium RGO:03023 RGO:03024 pancreatic calculus RGO:03024 prostatic calculi RGO:03026 prostatic calculus RGO:03026 SNOMEDCT:53898005 RGO:03032 lithopedion RGO:03032 RGO:03033 mineral oil granuloma RGO:03033 RGO:03036 urachal calculus RGO:03036 DOID:9589 SNOMEDCT:20342001 RGO:03037 urethral calculus RGO:03037 RGO:03038 widespread abdominal calcifications RGO:03038 RGO:03048 undifferentiated abdominal malignancy RGO:03048 RGO:03049 abdominal wall calcification RGO:03049 RADLEX:RID49692 SNOMEDCT:238888007 SNOMEDCT:79682009 RGO:03050 fat necrosis RGO:03050 RGO:03058 abdominal wall mass RGO:03058 ORDO:490 SNOMEDCT:80880002 RGO:03062 omphalomesenteric cyst RGO:03062 HP:0012618 ORDO:488 SNOMEDCT:17234001 RGO:03064 urachal cyst RGO:03064 RGO:03066 dilated bladder RGO:03066 DOID:11111 HP:0000126 RADLEX:RID34393 SNOMEDCT:43064006 RGO:03068 hydronephrosis RGO:03068 DOID:2974 HP:0000003 ICD10CM:Q61.4 SNOMEDCT:82525005 RGO:03069 multicystic dysplastic kidney RGO:03069 RGO:03071 enteric duplication cyst RGO:03071 HP:0012621 ICD10CM:Q43.7 SNOMEDCT:74829002 RGO:03074 persistent cloaca RGO:03074 HP:0030423 SNOMEDCT:79040006 RGO:03075 splenic cyst RGO:03075 DOID:12639 HP:0002021 RADLEX:RID46040 SNOMEDCT:367403001 RGO:03085 pyloric stenosis RGO:03085 RGO:03092 infantile polycystic kidneys RGO:03092 SNOMEDCT:128235003 RGO:03106 abdominal lymphadenopathy RGO:03106 RGO:03108 cavitary mesenteric lymph node syndrome RGO:03108 RGO:03112 pyogenic infection RGO:03112 XGP DOID:11401 RADLEX:RID3707 SNOMEDCT:38898003 RGO:03123 xanthogranulomatous pyelonephritis RGO:03123 RGO:03131 abnormal abdominal vessels RGO:03131 HP:0002617 RADLEX:RID3321 SNOMEDCT:432119003 SNOMEDCT:85659009 RGO:03132 aneurysm RGO:03132 DOID:2389 RADLEX:RID3309 SNOMEDCT:31653004 RGO:03136 fibromuscular dysplasia RGO:03136 azygos continuation azygos continuation of IVC azygos continuation of interrupted inferior vena cava ICD10CM:Q26.8 ORDO:99121 RADLEX:RID34583 RGO:03143 azygos continuation of inferior vena cava RGO:03143 HP:0004974 ORDO:1456 RGO:03144 coarctation of abdominal aorta RGO:03144 RGO:03147 portal vein occlusion RGO:03147 RGO:03151 A-alpha-lipoproteinemia RGO:03151 SNOMEDCT:59925007 RGO:03152 South American blastomycosis RGO:03152 DOID:2609 RADLEX:RID4525 SNOMEDCT:40293003 RGO:03153 adenomyoma RGO:03153 RGO:03155 assisted respiration RGO:03155 RGO:03156 emotional distress RGO:03156 HP:0002883 ICD10CM:R06.4 SNOMEDCT:68978004 RGO:03157 hyperventilation RGO:03157 SNOMEDCT:28263002 SNOMEDCT:304534000 RGO:03158 crying RGO:03158 RGO:03159 meat impaction RGO:03159 SNOMEDCT:66953006 RGO:03160 Ascaris RGO:03160 RADLEX:RID5635 RGO:03162 coin RGO:03162 RGO:03163 angiostrongyliasis costaricensis RGO:03163 RGO:03165 postrepair aorticoduodenal fistula RGO:03165 RGO:03168 angiomatous malformation RGO:03168 RGO:03171 carbonated beverages RGO:03171 RGO:03172 sodium bicarbonate ingestion RGO:03172 RADLEX:RID34880 RGO:03173 double-contrast barium enema RGO:03173 RGO:03174 gas pills RGO:03174 RADLEX:RID5253 SNOMEDCT:40857009 RGO:03176 cathartic colon RGO:03176 RADLEX:RID3434 RGO:03177 caustic colitis RGO:03177 celiac sprue coeliac disease gluten-induced enteropathy nontropical sprue DOID:10608 HP:0002608 ICD10CM:K90.0 RADLEX:RID5277 SNOMEDCT:396331005 RGO:03178 celiac disease RGO:03178 HP:0012450 ICD10CM:K59.09 SNOMEDCT:236069009 RGO:03179 chronic constipation RGO:03179 HP:0001399 SNOMEDCT:59927004 RGO:03180 liver failure RGO:03180 DOID:13767 ICD10CM:B66.1 SNOMEDCT:11938002 RGO:03181 clonorchiasis RGO:03181 DOID:885 ICD10CM:B66.3 SNOMEDCT:111922007 RGO:03182 fascioliasis RGO:03182 RGO:03183 colonic irrigation RGO:03183 RGO:03184 hydrogen peroxide enema RGO:03184 contrast agent contrast media RGO:03185 contrast medium RGO:03185 RADLEX:RID11872 SNOMEDCT:39290007 SNOMEDCT:426728000 RGO:03186 barium RGO:03186 RADLEX:RID3418 SNOMEDCT:64613007 RGO:03187 enteritis RGO:03187 DOID:6180 RGO:03188 cytomegalovirus gastritis RGO:03188 RGO:03189 cytomegalovirus antritis RGO:03189 SNOMEDCT:43387009 RGO:03190 fetus in fetu RGO:03190 SNOMEDCT:420422005 RGO:03191 diabetic acidosis RGO:03191 SNOMEDCT:111558006 RGO:03192 insulin shock RGO:03192 RGO:03195 pseudodiverticulosis RGO:03195 RGO:03196 duodenal atresia or stenosis RGO:03196 RGO:03197 emotional state alteration RGO:03197 RGO:03198 emotional states RGO:03198 DOID:8689 ICD10CM:F50.0 SNOMEDCT:56882008 RGO:03199 anorexia nervosa RGO:03199 RGO:03201 fecal matter RGO:03201 RGO:03202 pill ingestion RGO:03202 SNOMEDCT:39102003 RGO:03203 food particle RGO:03203 RGO:03204 adenomatous hyperplastic nodule RGO:03204 RGO:03205 fruit pit RGO:03205 RGO:03206 food particles RGO:03206 SNOMEDCT:264337003 RGO:03207 seeds RGO:03207 RGO:03208 air bubbles RGO:03208 RGO:03209 foreign bodies RGO:03209 SNOMEDCT:19227008 RGO:03211 foreign material RGO:03211 HP:0011856 RADLEX:RID779 SNOMEDCT:14077003 SNOMEDCT:423790006 RGO:03212 pica RGO:03212 SNOMEDCT:22907001 RGO:03214 heavy metal RGO:03214 DOID:3414 ICD10CM:E77.1 SNOMEDCT:65524005 RGO:03216 mannosidosis RGO:03216 SNOMEDCT:75258004 RGO:03218 food poisoning RGO:03218 DOID:3211 RADLEX:RID34414 RGO:03221 lysosomal storage disease RGO:03221 RGO:03223 hypertrophied prepyloric antral fold RGO:03223 DOID:0001816 HP:0200058 ORDO:263413 RADLEX:RID3989 SNOMEDCT:39000009 SNOMEDCT:403977003 RGO:03225 angiosarcoma RGO:03225 RADLEX:RID34646 SNOMEDCT:37876005 RGO:03226 phlebolith RGO:03226 RGO:03227 multiple transfusion effect RGO:03227 DOID:2230 ORDO:448 SNOMEDCT:408442008 SNOMEDCT:90935002 RGO:03228 hemophilia RGO:03228 ICD10CM:D67 SNOMEDCT:41788008 RGO:03229 Christmas disease RGO:03229 SNOMEDCT:70921007 RGO:03231 adenomatosis RGO:03231 RGO:03232 hydropneumometrocolpos RGO:03232 ICD10CM:K82.1 SNOMEDCT:78793006 RGO:03237 mucocele of gallbladder RGO:03237 ICD10CM:N70.1 SNOMEDCT:21711003 RGO:03238 hydrosalpinx RGO:03238 DOID:5732 SNOMEDCT:397810006 RGO:03239 pyosalpinx RGO:03239 RGO:03242 idiopathic calcinosis RGO:03242 infantile pyloric hypertrophy DOID:12638 RADLEX:RID5035 RGO:03243 hypertrophic pyloric stenosis RGO:03243 cast syndrome SNOMEDCT:257884004 RGO:03244 immobilization RGO:03244 DOID:10488 HP:0002023 ICD10CM:Q42.3 SNOMEDCT:204731006 RGO:03246 imperforate anus RGO:03246 HP:0002025 SNOMEDCT:69914001 RGO:03248 anal stenosis RGO:03248 RGO:03249 ileal prolapse RGO:03249 RGO:03250 ischemic gastritis RGO:03250 RGO:03252 generalized juvenile polyposis RGO:03252 DOID:127 RADLEX:RID4389 SNOMEDCT:146801000119103 SNOMEDCT:44598004 RGO:03253 leiomyoma RGO:03253 DOID:962 ORDO:252183 RADLEX:RID4462 SNOMEDCT:404029005 SNOMEDCT:89084002 RGO:03254 neurofibroma RGO:03254 DOID:8584 HP:0030080 ICD10CM:C83.7 ORDO:543 SNOMEDCT:118617000 SNOMEDCT:77381001 RGO:03256 Burkitt lymphoma RGO:03256 DOID:3153 HP:0001012 RADLEX:RID5219 SNOMEDCT:37095002 SNOMEDCT:402693001 RGO:03257 lipomatosis RGO:03257 DOID:3382 HP:0012034 ORDO:69078 RADLEX:RID4358 SNOMEDCT:254829001 SNOMEDCT:49430005 RGO:03258 liposarcoma RGO:03258 RGO:03259 extrauterine pregnancy RGO:03259 LAM DOID:3319 HP:0012798 ICD10CM:J84.81 ORDO:538 RADLEX:RID4372 SNOMEDCT:73017001 RGO:03260 lymphangioleiomyomatosis RGO:03260 SNOMEDCT:446688004 RGO:03263 leukemic infiltration RGO:03263 Hodgkin lymphoma DOID:8567 HP:0012189 SNOMEDCT:118599009 RGO:03264 Hodgkin disease RGO:03264 RADLEX:RID4900 SNOMEDCT:30477007 RGO:03267 internal hernia RGO:03267 RGO:03268 inguinal or femoral hernia RGO:03268 ICD10CM:K55.9 SNOMEDCT:73665001 RGO:03269 ischemic enteritis RGO:03269 RGO:03270 extension from carcinoma of pancreas RGO:03270 RGO:03271 invasion from adjacent neoplasm RGO:03271 DOID:9884 HP:0003560 ICD10CM:G71.0 SNOMEDCT:73297009 RGO:03276 muscular dystrophy RGO:03276 RGO:03277 perinatal omphalitis RGO:03277 SNOMEDCT:43961000 RGO:03280 nodular lymphoid hyperplasia RGO:03280 DOID:0060327 HP:0001539 ICD10CM:Q79.2 ORDO:660 SNOMEDCT:18735004 RGO:03281 omphalocele RGO:03281 RGO:03282 pancreatitis with saponification RGO:03282 DOID:8506 ICD10CM:L12.0 ORDO:703 SNOMEDCT:77090002 RGO:03284 bullous pemphigoid RGO:03284 RGO:03285 hyperacidity RGO:03285 SNOMEDCT:80640009 RGO:03286 perinephric abscess RGO:03286 DOID:11400 HP:0012330 ICD10CM:N16 RADLEX:RID3547 SNOMEDCT:45816000 RGO:03287 pyelonephritis RGO:03287 SNOMEDCT:387715005 RGO:03288 peritoneal lavage RGO:03288 RGO:03290 phleboliths RGO:03290 RGO:03291 physiologic reflux at ampulla RGO:03291 RGO:03292 incompetent sphincter RGO:03292 SNOMEDCT:238383006 RGO:03293 stitch abscess RGO:03293 RGO:03294 prolapsed gastrostomy tube RGO:03294 instrument instrumentation of bladder recent instrumentation SNOMEDCT:309824003 RGO:03295 instrumentation RGO:03295 RGO:03296 post-traumatic cyst RGO:03296 RGO:03297 pancreatic fracture RGO:03297 RGO:03300 pseudodefect in neck of gallbladder RGO:03300 DOID:12679 HP:0000121 SNOMEDCT:48638002 RGO:03303 nephrocalcinosis RGO:03303 DOID:1074 HP:0000083 RADLEX:RID5307 SNOMEDCT:42399005 RGO:03304 renal failure RGO:03304 DOID:4676 RADLEX:RID5308 SNOMEDCT:44730006 RGO:03305 uremia RGO:03305 SNOMEDCT:19351000 RGO:03306 acute glomerulonephritis RGO:03306 SNOMEDCT:52765003 RGO:03307 intubation RGO:03307 HP:0030736 SNOMEDCT:281561000 RGO:03308 sacrococcygeal teratoma RGO:03308 SNOMEDCT:125666000 SNOMEDCT:48333001 RGO:03311 burn RGO:03311 DOID:10223 ORDO:221 RADLEX:RID34666 SNOMEDCT:396230008 RGO:03312 dermatomyositis RGO:03312 DOID:3488 HP:0100658 RADLEX:RID34641 SNOMEDCT:128045006 SNOMEDCT:385627004 RGO:03313 cellulitis RGO:03313 HP:0031273 SNOMEDCT:27942005 RGO:03314 shock RGO:03314 RGO:03315 gram-negative septicemia RGO:03315 SNOMEDCT:389086002 RGO:03316 hypoxia RGO:03316 RGO:03317 septicemia RGO:03317 HP:0200036 SNOMEDCT:95319004 RGO:03319 skin nodule RGO:03319 RADLEX:RID5627 SNOMEDCT:341000119102 RGO:03320 tattoo RGO:03320 RGO:03321 colostomy orifice RGO:03321 SNOMEDCT:257159000 RGO:03322 debris RGO:03322 HP:0100561 RGO:03323 spinal cord lesion RGO:03323 DOID:607 HP:0010550 ICD10CM:G82.2 SNOMEDCT:60389000 RGO:03324 paraplegia RGO:03324 RGO:03325 splenic laceration RGO:03325 RGO:03326 pericapsular hematoma RGO:03326 DOID:10607 ICD10CM:K90.1 RADLEX:RID5280 SNOMEDCT:47384003 RGO:03327 tropical sprue RGO:03327 RADLEX:RID34787 SNOMEDCT:128561003 RGO:03332 granulomatous disease RGO:03332 SNOMEDCT:55025003 RGO:03333 uremic colitis RGO:03333 SNOMEDCT:70153002 RGO:03335 hemorrhoids RGO:03335 DOID:9746 SNOMEDCT:70153002 RGO:03336 hemorrhoid RGO:03336 RGO:03337 vascular occlusion RGO:03337 HP:0002013 ICD10CM:R11.1 RADLEX:RID39186 SNOMEDCT:422400008 RGO:03338 vomiting RGO:03338 SNOMEDCT:48026007 RGO:03339 inanition RGO:03339 DOID:0060125 ICD10CM:C88.2 ORDO:86864 SNOMEDCT:6381009 SNOMEDCT:68979007 RGO:03340 heavy chain disease RGO:03340 lower esophageal ring RADLEX:RID5027 SNOMEDCT:66889002 RGO:03343 Schatzki ring RGO:03343 SNOMEDCT:80640009 RGO:03344 perirenal abscess RGO:03344 DKA DOID:1837 HP:0001953 SNOMEDCT:420422005 RGO:03346 diabetic ketoacidosis RGO:03346 SNOMEDCT:26298008 RGO:03347 diabetic coma RGO:03347 RGO:03348 bladder distended with air RGO:03348 SNOMEDCT:52123000 RGO:03349 emphysematous cystitis RGO:03349 RGO:03355 Pro-Banthine RGO:03355 SNOMEDCT:372832002 SNOMEDCT:73949004 RGO:03356 atropine RGO:03356 RADLEX:RID45794 SNOMEDCT:373529000 SNOMEDCT:73572009 RGO:03357 morphine RGO:03357 RGO:03358 Lomotil RGO:03358 SNOMEDCT:264519003 SNOMEDCT:62014003 RGO:03359 drug reaction RGO:03359 RGO:03360 granulomatous esophagitis RGO:03360 RGO:03364 primary anemia RGO:03364 HP:0005240 ICD10CM:K22.2 RGO:03365 esophageal obstruction RGO:03365 DOID:6297 SNOMEDCT:235603003 RGO:03366 viral esophagitis RGO:03366 RGO:03367 herpes RGO:03367 SNOMEDCT:8098009 RGO:03370 sexually transmitted disease RGO:03370 RGO:03372 chronic colonic obstruction RGO:03372 SNOMEDCT:83821001 RGO:03373 Cryptosporidium RGO:03373 SNOMEDCT:111812000 RGO:03375 atypical mycobacterial infection RGO:03375 RGO:03377 AIDS-related neoplasm RGO:03377 SNOMEDCT:10573002 RGO:03378 amnionitis RGO:03378 DOID:1002 RADLEX:RID3417 SNOMEDCT:78623009 RGO:03379 endometritis RGO:03379 RGO:03380 physometra RGO:03380 RGO:03381 infected fetus RGO:03381 DOID:2349 HP:0002634 RADLEX:RID3285 SNOMEDCT:28960008 RGO:03382 arteriosclerosis RGO:03382 RGO:03383 acquired aortic abnormality RGO:03383 SNOMEDCT:360441005 RGO:03385 aganglionosis of colon RGO:03385 RGO:03387 distention of stomach RGO:03387 SNOMEDCT:386831001 RGO:03388 gastroscopy RGO:03388 RGO:03390 misplaced oxygen tube RGO:03390 HP:0012089 RADLEX:RID3682 SNOMEDCT:52089001 RGO:03391 arteritis RGO:03391 aortic arch syndrome aortitis syndrome aortoarteritis middle aortic syndrome pulseless disease DOID:2508 ORDO:3287 RADLEX:RID3694 RGO:03392 Takayasu arteritis RGO:03392 DOID:9810 ICD10CM:M30.0 ORDO:767 RADLEX:RID3692 SNOMEDCT:155441006 RGO:03393 polyarteritis nodosa RGO:03393 RGO:03394 granulomatous infiltration of stomach wall RGO:03394 DOID:583 HP:0001878 RADLEX:RID34678 SNOMEDCT:61261009 RGO:03396 hemolytic anemia RGO:03396 DOID:14018 SNOMEDCT:420054005 RGO:03397 alcoholic cirrhosis RGO:03397 DOID:12236 HP:0002613 ICD10CM:K74.3 ORDO:186 RADLEX:RID3823 SNOMEDCT:31712002 RGO:03398 primary biliary cirrhosis RGO:03398 PID DOID:1003 RADLEX:RID3716 SNOMEDCT:198130006 RGO:03400 pelvic inflammatory disease RGO:03400 interposition of colon between liver and right hemidiaphragm RADLEX:RID35978 RGO:03402 Chilaiditi syndrome RGO:03402 atrophic liver hepatic atrophy RGO:03404 liver atrophy RGO:03404 DOID:10021 RGO:03407 duodenal neoplasm RGO:03407 DOID:11963 HP:0100633 ICD10CM:K20 RADLEX:RID3440 SNOMEDCT:16761005 RGO:03408 esophagitis RGO:03408 RGO:03410 chronic fibrosing mesenteritis RGO:03410 ICD10CM:K65.4 RGO:03411 mesenteric lipodystrophy RGO:03411 DOID:1526 HP:0012490 RADLEX:RID3532 SNOMEDCT:22125009 RGO:03412 panniculitis RGO:03412 retroperitoneal fat deposition RGO:03413 retroperitoneal lipomatosis RGO:03413 lipomatosis of renal sinus RGO:03414 renal sinus lipomatosis RGO:03414 RGO:03416 malabsorption syndromes RGO:03416 SNOMEDCT:86341008 RGO:03417 vascular insufficiency RGO:03417 RGO:03420 tortuous artery RGO:03420 RGO:03421 thickening of root of mesentery RGO:03421 RGO:03424 tuberculous colitis RGO:03424 DOID:7814 SNOMEDCT:235749000 RGO:03425 cytomegalovirus colitis RGO:03425 RGO:03426 late-stage paralytic strongyloidiasis RGO:03426 Minkowski-Chauffard disease HP:0004444 SNOMEDCT:17235000 RGO:03428 spherocytosis RGO:03428 RADLEX:RID5022 SNOMEDCT:27551008 RGO:03429 stricture RGO:03429 RGO:03430 lye stricture RGO:03430 RGO:03431 congenital esophageal web RGO:03431 ICD10CM:D50.1 ORDO:54028 SNOMEDCT:80126007 RGO:03432 Plummer-Vinson syndrome RGO:03432 DOID:437 ICD10CM:G70.0 ORDO:589 SNOMEDCT:91637004 RGO:03435 myasthenia gravis RGO:03435 SNOMEDCT:26715006 RGO:03436 steroid myopathy RGO:03436 RGO:03437 oculopharyngeal myopathy RGO:03437 SNOMEDCT:68437005 RGO:03438 thyrotoxic myopathy RGO:03438 DOID:9786 RGO:03441 bulbar poliomyelitis RGO:03441 RGO:03442 high unilateral cervical vagotomy RGO:03442 DOID:2377 ICD10CM:G35 RADLEX:RID28801 SNOMEDCT:24700007 RGO:03443 multiple sclerosis RGO:03443 HP:0001300 SNOMEDCT:32798002 RGO:03444 parkinsonism RGO:03444 DOID:332 HP:0007354 ICD10CM:G12.21 ORDO:803 RADLEX:RID5128 SNOMEDCT:86044005 RGO:03446 amyotrophic lateral sclerosis RGO:03446 DOID:11405 ICD10CM:A36 ORDO:1679 SNOMEDCT:397428000 RGO:03451 diphtheria RGO:03451 RGO:03453 pharyngeal abscess RGO:03453 SNOMEDCT:23166004 RGO:03454 pharyngeal cellulitis RGO:03454 DOID:12765 ICD10CM:J36 SNOMEDCT:15033003 RGO:03455 peritonsillar abscess RGO:03455 SNOMEDCT:102453009 RGO:03456 peritonsillar cellulitis RGO:03456 HP:0001283 SNOMEDCT:54304004 RGO:03457 bulbar palsy RGO:03457 DOID:12680 HP:0007024 SNOMEDCT:7379000 RGO:03458 pseudobulbar palsy RGO:03458 DOID:3817 HP:0006824 SNOMEDCT:73013002 RGO:03459 cranial nerve palsy RGO:03459 DOID:11634 SNOMEDCT:43153006 RGO:03463 myxedema RGO:03463 esophageal motility disorder DOID:9192 SNOMEDCT:266434009 RGO:03464 esophageal dysmotility RGO:03464 DOID:5517 RADLEX:RID4251 SNOMEDCT:372143007 RGO:03466 gastric carcinoma RGO:03466 DOID:11920 DOID:248 HP:0100551 RGO:03467 tracheal neoplasm RGO:03467 RGO:03468 left main stem bronchus RGO:03468 RGO:03469 confluence of left pulmonary veins RGO:03469 RGO:03470 extrinsic impression on thoracic esophagus RGO:03470 RGO:03471 extrinsic impression on the cervical esophagus RGO:03471 DOID:3892 HP:0012197 ORDO:97279 RADLEX:RID4486 SNOMEDCT:25324008 SNOMEDCT:302822000 RGO:03472 insulinoma RGO:03472 DOID:5577 RADLEX:RID4484 SNOMEDCT:16189002 SNOMEDCT:302824004 RGO:03473 gastrinoma RGO:03473 HP:0030404 ORDO:97280 RADLEX:RID4485 SNOMEDCT:128855009 SNOMEDCT:302823005 RGO:03474 glucagonoma RGO:03474 DOID:4430 ORDO:97283 RADLEX:RID4497 SNOMEDCT:128642005 SNOMEDCT:253006001 RGO:03475 somatostatinoma RGO:03475 DOID:5574 ORDO:97282 RADLEX:RID4498 SNOMEDCT:31131002 SNOMEDCT:447643008 RGO:03476 VIPoma RGO:03476 RGO:03477 nonfunctioning islet cell tumor RGO:03477 pancreatic divisum HP:0030994 SNOMEDCT:54554009 RGO:03479 pancreas divisum RGO:03479 RGO:03481 vascular impression RGO:03481 HP:0012020 ICD10CM:Q25.47 ORDO:99081 SNOMEDCT:111321007 SNOMEDCT:244229003 RGO:03482 right aortic arch RGO:03482 RGO:03484 opportunistic esophagitis RGO:03484 monilial esophagitis DOID:13146 RGO:03485 candida esophagitis RGO:03485 RGO:03486 herpes esophagitis RGO:03486 DOID:7706 SNOMEDCT:713045003 RGO:03487 cytomegalovirus esophagitis RGO:03487 RGO:03488 extrinsic compression RGO:03488 RGO:03490 neurenteric duplication cyst RGO:03490 RGO:03491 bronchogenic duplication cyst RGO:03491 HP:0031014 RGO:03493 aberrant right subclavian artery RGO:03493 RGO:03494 aberrant left subclavian artery RGO:03494 HP:0002043 SNOMEDCT:63305008 RGO:03495 esophageal stricture RGO:03495 RGO:03496 congenital esophageal stricture RGO:03496 RGO:03497 strictire secondary to esophagitis RGO:03497 RGO:03502 peripheral or central cranial nerve palsy RGO:03502 DOID:10222 ICD10CM:M33.2 ORDO:732 RADLEX:RID3654 SNOMEDCT:31384009 RGO:03506 polymyositis RGO:03506 SLE lupus lupus erythematosus DOID:9074 HP:0002725 SNOMEDCT:55464009 RGO:03509 systemic lupus erythematosus RGO:03509 RA DOID:7148 HP:0001370 RADLEX:RID3561 SNOMEDCT:69896004 RGO:03510 rheumatoid arthritis RGO:03510 RGO:03511 infiltrative neoplasm RGO:03511 RGO:03512 diffuse esophageal carcinoma RGO:03512 RGO:03514 sclerotherapy for varices RGO:03514 RGO:03518 superficial spreading carcinoma of esophagus RGO:03518 RGO:03519 inflammatory disease of duodenum RGO:03519 RGO:03520 prolapsed gastric lesion RGO:03520 RGO:03521 prolapsed gastric polyp RGO:03521 RGO:03522 duodenal stricture RGO:03522 Ladd bands SNOMEDCT:29642000 RGO:03523 congenital peritoneal bands RGO:03523 RGO:03524 Ascaris bolus RGO:03524 DOID:10718 SNOMEDCT:58265007 RGO:03525 giardiasis RGO:03525 RGO:03526 primary neoplasm of duodenum RGO:03526 RGO:03528 metastatic neoplasm of duodenum RGO:03528 SNOMEDCT:56457002 RGO:03529 congenital atresia RGO:03529 RADLEX:RID5016 SNOMEDCT:415582006 RGO:03531 stenosis RGO:03531 SNOMEDCT:297165008 RGO:03534 duodenal diaphragm RGO:03534 RGO:03537 sluggish bowel transit RGO:03537 RADLEX:RID6432 SNOMEDCT:257750007 RGO:03539 side-to-side anastomosis RGO:03539 RADLEX:RID1695 RGO:03540 gastroileostomy RGO:03540 RGO:03541 bypass procedure RGO:03541 DOID:10605 RADLEX:RID4609 SNOMEDCT:26629001 RGO:03542 short bowel syndrome RGO:03542 RADLEX:RID4931 SNOMEDCT:60627008 RGO:03543 obturator hernia RGO:03543 HMD hyaline membrane disease ORDO:70587 RGO:03544 infantile respiratory distress syndrome RGO:03544 RGO:03545 esophageal surgery RGO:03545 RGO:03546 pulmonary surgery RGO:03546 SNOMEDCT:77515003 RGO:03547 curare RGO:03547 infantile gastroesophageal regurgitation SNOMEDCT:65453009 RGO:03548 chalasia RGO:03548 RGO:03550 surgical repair of esophageal atresia RGO:03550 RGO:03551 surgical repair of hiatal hernia RGO:03551 RGO:03552 surgical repair of tracheoesophageal fistula RGO:03552 RGO:03554 pericholecystic fluid RGO:03554 RGO:03555 gallbladder torsion RGO:03555 RGO:03556 distended gallbladder in a child RGO:03556 upper esophageal diverticulum RGO:03557 diverticulum of upper esophagus RGO:03557 RGO:03559 communicating duplication cyst RGO:03559 SNOMEDCT:371139006 RGO:03560 early cirrhosis RGO:03560 SNOMEDCT:4584002 RGO:03561 scirrhous carcinoma RGO:03561 RGO:03563 late ischemic colitis RGO:03563 RGO:03564 late radiation colitis RGO:03564 enlarged spleen HP:0001744 RADLEX:RID34587 SNOMEDCT:16294009 RGO:03565 splenomegaly RGO:03565 RGO:03566 gastric bezoar RGO:03566 SNOMEDCT:26345007 RGO:03567 disseminated histoplasmosis RGO:03567 DOID:0060321 HP:0001537 ICD10CM:K42 RADLEX:RID4915 SNOMEDCT:396347007 RGO:03568 umbilical hernia RGO:03568 HP:0002933 ICD10CM:K43 RADLEX:RID4917 SNOMEDCT:414396006 RGO:03569 ventral hernia RGO:03569 obstruction of duodenum DOID:3558 RGO:03570 duodenal obstruction RGO:03570 HP:0004791 RGO:03575 esophageal ulceration RGO:03575 RGO:03576 gastroesophageal regurgitation RGO:03576 RGO:03577 bowel infarction RGO:03577 intestinal ischemia ischemic bowel ischemic bowel disease ischemic enterocolitis mesenteric ischemia mesenteric ischemia or infarction RGO:03578 bowel ischemia RGO:03578 localized ileus RGO:03579 sentinel loop RGO:03579 appendicitis DOID:8337 ICD10CM:K35 SNOMEDCT:85189001 RGO:03580 acute appendicitis RGO:03580 RGO:03582 acute ureteral colic RGO:03582 DOID:752 RGO:03583 perforated peptic ulcer RGO:03583 HP:0002097 ICD10CM:J43 RADLEX:RID4799 SNOMEDCT:49158009 RGO:03584 emphysema RGO:03584 RGO:03585 abnormal position of stomach RGO:03585 SNOMEDCT:53326005 RGO:03587 Candida albicans RGO:03587 lateral pharyngeal pouch RGO:03588 pharyngocele RGO:03588 diverticulosis of small bowel RGO:03592 small bowel diverticulosis RGO:03592 RADLEX:RID1607 SNOMEDCT:72791001 RGO:03594 laryngectomy RGO:03594 RGO:03595 upper lobectomy RGO:03595 RGO:03596 neck infection RGO:03596 RGO:03597 acquired pharyngocele RGO:03597 RGO:03598 glass blowing RGO:03598 RGO:03599 trumpet playing RGO:03599 RGO:03600 traction diverticulum of upper esophagus RGO:03600 RGO:03601 intramural esophageal hemorrhage RGO:03601 RGO:03602 small bowel wall thickening RGO:03602 DOID:0050230 ICD10CM:B81.1 SNOMEDCT:23949002 RGO:03603 intestinal capillariasis RGO:03603 SNOMEDCT:359762003 RGO:03604 hookworm RGO:03604 SNOMEDCT:112283007 RGO:03605 E. coli RGO:03605 SNOMEDCT:34872001 RGO:03606 vibrio RGO:03606 RGO:03607 mucosal destruction of small bowel RGO:03607 DOID:12662 ICD10CM:B41 ORDO:73260 SNOMEDCT:59925007 RGO:03608 paracoccidioidomycosis RGO:03608 RGO:03609 hookworm disease RGO:03609 HP:0003075 SNOMEDCT:8900005 RGO:03610 hypoproteinemia RGO:03610 DOID:2527 HP:0000100 SNOMEDCT:90708001 RGO:03611 nephrosis RGO:03611 RGO:03612 dysproteinemia RGO:03612 RGO:03613 small bowel edema RGO:03613 ORDO:90363 SNOMEDCT:715667003 SNOMEDCT:717255008 RGO:03614 secondary intestinal lymphangiectasia RGO:03614 RGO:03615 mesenteric neoplasm RGO:03615 HP:0004387 SNOMEDCT:43752006 RGO:03616 enterocolitis RGO:03616 DOID:12133 RGO:03617 Yersinia enterocolitis RGO:03617 RGO:03618 intramural hemorrhage of small bowel RGO:03618 RGO:03619 bleeding or clotting disorder RGO:03619 HP:0002615 ICD10CM:I95 RADLEX:RID34689 SNOMEDCT:45007003 RGO:03621 hypotension RGO:03621 SNOMEDCT:84210007 RGO:03622 Campylobacter fetus RGO:03622 SNOMEDCT:66543000 RGO:03623 Campylobacter jejuni RGO:03623 SNOMEDCT:58503001 RGO:03624 Mycobacterium avium-intracellulare RGO:03624 RGO:03628 chronic duodenal ulcer disease RGO:03628 RGO:03629 necrotic tumor with perforation RGO:03629 ICD10CM:K51.0 RADLEX:RID3419 RGO:03630 backwash ileitis RGO:03630 HP:0004401 RADLEX:RID5272 SNOMEDCT:206523001 RGO:03640 meconium ileus RGO:03640 RGO:03641 ulcerative coliitis with toxic megacolon RGO:03641 RGO:03642 segmental bowel wall thickening RGO:03642 RGO:03643 infectious enterocolitis RGO:03643 RGO:03644 mucinous carcinoma of colon RGO:03644 RGO:03645 colloid carcinoma of colon RGO:03645 RGO:03646 scirrhous carcinoma of colon RGO:03646 RGO:03647 scirrhous carcinoma of rectum RGO:03647 RGO:03648 segmental narrowing of colon RGO:03648 RGO:03649 herpes colitis RGO:03649 RGO:03650 fungal colitis RGO:03650 vitamin E depletion RGO:03651 ceroidosis RGO:03651 SNOMEDCT:49839002 RGO:03652 hexamethonium RGO:03652 SNOMEDCT:387258005 SNOMEDCT:47331002 RGO:03653 chlorpromazine RGO:03653 SNOMEDCT:372846002 SNOMEDCT:77390008 RGO:03654 benztropine RGO:03654 levodopa SNOMEDCT:65955006 RGO:03655 L-DOPA RGO:03655 SNOMEDCT:105593004 RGO:03659 electrolyte imbalance RGO:03659 RGO:03660 lead colic RGO:03660 DOID:10922 SNOMEDCT:417425009 RGO:03661 sickle cell crisis RGO:03661 DOID:14330 RADLEX:RID5163 SNOMEDCT:49049000 RGO:03666 Parkinson disease RGO:03666 SNOMEDCT:271873000 SNOMEDCT:32864002 RGO:03667 senility RGO:03667 DOID:5419 HP:0100753 ICD10CM:F20 SNOMEDCT:58214004 RGO:03668 schizophrenia RGO:03668 RADLEX:RID34755 SNOMEDCT:127294003 SNOMEDCT:2470005 RGO:03669 brain damage RGO:03669 HP:0003470 RADLEX:RID5256 SNOMEDCT:44695005 RGO:03670 paralysis RGO:03670 DOID:552 HP:0002090 RADLEX:RID5350 SNOMEDCT:233604007 RGO:03672 pneumonia RGO:03672 RGO:03674 psychogenic megacolon RGO:03674 SNOMEDCT:197139005 RGO:03675 idiopathic megacolon RGO:03675 DOID:2394 HP:0100615 RGO:03676 ovarian neoplasm RGO:03676 RGO:03677 iliac artery aneurysm RGO:03677 RGO:03680 paralysis of left hemidiaphragm RGO:03680 RADLEX:RID4899 SNOMEDCT:3662000 RGO:03681 paraesophageal hernia RGO:03681 HP:0025194 RADLEX:RID4938 RGO:03682 Morgagni hernia RGO:03682 HP:0025193 RGO:03683 Bochdalek hernia RGO:03683 RGO:03684 traumatic hernia RGO:03684 RGO:03685 intrapericardial hernia RGO:03685 SNOMEDCT:71851009 RGO:03686 gastric volvulus RGO:03686 RGO:03687 inversion of left hemidiaphragm RGO:03687 HP:0002202 RADLEX:RID34539 SNOMEDCT:60046008 RGO:03688 pleural effusion RGO:03688 RADLEX:RID43412 RGO:03689 thoracic mass RGO:03689 RGO:03690 enlarged left kidney RGO:03690 RGO:03691 enlarged pancreas RGO:03691 SNOMEDCT:235996002 RGO:03692 lesser sac abscess RGO:03692 HP:0100721 SNOMEDCT:52324001 RGO:03693 mediastinal lymphadenopathy RGO:03693 LA enlargement LAE HP:0031295 SNOMEDCT:67741000119109 RGO:03695 left atrial enlargement RGO:03695 RGO:03696 abnormal vascular impression on esophagus RGO:03696 DOID:14004 HP:0012727 RGO:03697 thoracic aortic aneurysm RGO:03697 RGO:03698 thoracic aortic tortuosity RGO:03698 DOID:4667 HP:0002808 RADLEX:RID4759 SNOMEDCT:414564002 RGO:03699 kyphosis RGO:03699 osteophytes DOID:203 ICD10CM:M25.7 RADLEX:RID5076 SNOMEDCT:88998003 RGO:03701 osteophyte RGO:03701 DOID:5612 RGO:03703 spinal neoplasm RGO:03703 RGO:03704 spinal osteomyelitis RGO:03704 RGO:03705 pulmonary mass RGO:03705 DOID:118 HP:0001698 RADLEX:RID38588 SNOMEDCT:373945007 RGO:03706 pericardial effusion RGO:03706 DOID:116 RGO:03708 pericardial tumor RGO:03708 DOID:5559 RGO:03709 mediastinal tumor RGO:03709 RGO:03710 mediastinal cyst RGO:03710 HH hiatus hernia DOID:12642 HP:0002036 RADLEX:RID4897 SNOMEDCT:84089009 RGO:03713 hiatal hernia RGO:03713 RGO:03722 lye ingestion RGO:03722 Candida infection moniliasis DOID:1508 ICD10CM:B37 SNOMEDCT:78048006 RGO:03724 candidiasis RGO:03724 DOID:8534 HP:0002020 RADLEX:RID5260 RGO:03725 gastroesophageal reflux RGO:03725 spontaneous esophageal mucosal tear ICD10CM:K22.6 SNOMEDCT:35265002 RGO:03738 Mallory-Weiss syndrome RGO:03738 RGO:03741 congenital pharyngocele RGO:03741 ORDO:90362 SNOMEDCT:6124009 RGO:03742 primary intestinal lymphangiectasia RGO:03742 HP:0003113 ICD10CM:E87.8 SNOMEDCT:10399008 RGO:03746 hypochloremia RGO:03746 RGO:03747 calcium abnormality RGO:03747 SNOMEDCT:11672007 RGO:03751 organoaxial gastric volvulus RGO:03751 SNOMEDCT:35865007 RGO:03752 mesenteroaxial gastric volvulus RGO:03752 sliding hiatal hernia RGO:03753 axial hiatal hernia RGO:03753 RGO:03760 retrolaryngeal abscess RGO:03760 RGO:03761 retrolaryngeal hematoma RGO:03761 SNOMEDCT:237557003 RGO:03764 thyroid mass RGO:03764 DOID:2891 HP:0000854 SNOMEDCT:255033000 RGO:03766 thyroid adenoma RGO:03766 carcinoma of thyroid DOID:3963 HP:0002890 RGO:03767 thyroid carcinoma RGO:03767 DOID:7166 HP:0100646 ICD10CM:E06 RADLEX:RID3666 SNOMEDCT:82119001 RGO:03768 thyroiditis RGO:03768 RADLEX:RID1029 RGO:03769 pharyngeal venous plexus RGO:03769 HP:0100751 RGO:03770 esophageal neoplasm RGO:03770 DOID:819 ICD10CM:J98.51 RADLEX:RID3490 SNOMEDCT:47597000 RGO:03772 mediastinitis RGO:03772 RGO:03773 nerve destruction by neoplasm RGO:03773 SNOMEDCT:405247003 RGO:03774 obstruction of esophagus RGO:03774 SNOMEDCT:126817006 RGO:03775 neoplasm of esophagus RGO:03775 RGO:03776 schwannoma of vagus nerve RGO:03776 RGO:03777 schwannoma of phrenic nerve RGO:03777 DISH Forestier disease ankylosing hyperostosis DOID:6652 RADLEX:RID5069 SNOMEDCT:31487001 RGO:03778 diffuse idiopathic skeletal hyperostosis RGO:03778 RGO:03779 pleuropulmonary fibrosis at lung apex RGO:03779 ICD10CM:Q20.5 SNOMEDCT:24016004 RGO:03782 corrected transposition RGO:03782 bronchopulmonary sequestration sequestration of lung HP:0100632 ORDO:3161 SNOMEDCT:18620009 RGO:03784 pulmonary sequestration RGO:03784 RGO:03785 enlarged bronchial artery RGO:03785 HP:0001660 ORDO:3384 SNOMEDCT:308828009 RGO:03786 truncus arteriosus RGO:03786 RGO:03787 absent main pulmonary artery RGO:03787 SNOMEDCT:426121003 RGO:03788 granulomatous lymphadenitis RGO:03788 RGO:03789 perforated diverticulum of esophagus RGO:03789 DOID:3905 RGO:03793 lung carcinoma RGO:03793 RGO:03794 tracheal carcinoma RGO:03794 SNOMEDCT:19995004 RGO:03796 spontaneous rupture of esophagus RGO:03796 SNOMEDCT:235627001 RGO:03797 traumatic rupture of esophagus RGO:03797 RGO:03798 iatrogenic rupture of esophagus RGO:03798 RGO:03799 intramural esophageal abscess RGO:03799 RADLEX:RID45710 SNOMEDCT:423827005 RGO:03800 endoscopy RGO:03800 RGO:03801 postgastrectomy alkaline reflux esophagitis RGO:03801 SNOMEDCT:54694004 RGO:03802 mobile cecum RGO:03802 RGO:03805 chronic bacillary dysentery RGO:03805 RGO:03806 amebic stricture RGO:03806 SNOMEDCT:23513009 RGO:03807 herpes infection RGO:03807 RGO:03808 aphthoid ulcer of bowel RGO:03808 RGO:03809 artifactual colon filling defect RGO:03809 RGO:03814 perforated neoplasm of colon RGO:03814 RGO:03815 suture leak RGO:03815 RGO:03816 talc granuloma RGO:03816 SNOMEDCT:385186005 SNOMEDCT:61919008 RGO:03817 enema RGO:03817 RGO:03819 plexiform neurofibromatosis RGO:03819 HP:0002475 SNOMEDCT:414667000 RGO:03820 meningomyelocele RGO:03820 DOID:0080016 HP:0002414 ICD10CM:Q05 RADLEX:RID34708 SNOMEDCT:67531005 RGO:03821 spina bifida RGO:03821 DOID:0080072 RADLEX:RID5292 SNOMEDCT:253783001 RGO:03822 neuronal intestinal dysplasia RGO:03822 SNOMEDCT:278926001 RGO:03828 psychogenic RGO:03828 RADLEX:RID5664 SNOMEDCT:54690008 RGO:03829 idiopathic RGO:03829 RGO:03830 distal obstructing lesion RGO:03830 RGO:03831 prolonged immobilization RGO:03831 RGO:03832 chronic colonic stricture RGO:03832 RGO:03833 postoperative scarring RGO:03833 NEC DOID:8677 ICD10CM:K55.3 RADLEX:RID3436 SNOMEDCT:2707005 RGO:03834 necrotizing enterocolitis RGO:03834 RGO:03836 anti-parkinsonism agent RGO:03836 shigellosis DOID:12385 SNOMEDCT:274081004 RGO:03837 bacillary dysentery RGO:03837 RGO:03838 acute bacillary dysentery RGO:03838 SNOMEDCT:423590009 RGO:03839 pseudomembranous enterocolitis RGO:03839 RGO:03840 hemorrhagic enterocolitis RGO:03840 SNOMEDCT:204700004 RGO:03842 congenital ileal stenosis RGO:03842 RGO:03843 congenital ileal web RGO:03843 RGO:03845 distal jejunal atresia RGO:03845 HP:0011102 SNOMEDCT:25896009 RGO:03846 ileal atresia RGO:03846 MMIH syndrome megacystis - microcolon - intestinal hypoperistalsis syndrome neonatal hollow visceral myopathy DOID:0060610 ORDO:2241 RGO:03848 Berdon syndrome RGO:03848 question-mark colon RGO:03849 total aganglionosis coli RGO:03849 RADLEX:RID153 SNOMEDCT:23153004 RGO:03851 ileocecal valve RGO:03851 RGO:03852 ileocecal valve lipoma RGO:03852 RGO:03853 ileocecal prolapse RGO:03853 SNOMEDCT:197049005 RGO:03854 ileocecal intussusception RGO:03854 RADLEX:RID168 SNOMEDCT:181255000 SNOMEDCT:66754008 RGO:03855 normal appendix RGO:03855 DOID:1252 ICD10CM:B79 SNOMEDCT:3752003 RGO:03856 trichuriasis RGO:03856 RGO:03857 solitary ulcer RGO:03857 SNOMEDCT:430347001 RGO:03858 diverticulitis of cecum RGO:03858 enlargement of ileocecal valve RGO:03859 enlarged ileocecal valve RGO:03859 RGO:03860 impacted gallstone RGO:03860 RGO:03861 impacted foreign body RGO:03861 lipomatosis of ileocecal valve SNOMEDCT:6241000 RGO:03863 fatty infiltration of ileocecal valve RGO:03863 RGO:03865 anterior indentation on rectosigmoid junction RGO:03865 DOID:0050918 ORDO:180247 RGO:03866 vaginal carcinoma RGO:03866 ICD10CM:N89.7 SNOMEDCT:26228000 RGO:03867 hematocolpos RGO:03867 DOID:1285 RGO:03868 rectal disease RGO:03868 DOID:3127 SNOMEDCT:3951002 RGO:03870 proctitis RGO:03870 SNOMEDCT:52231000 RGO:03871 idiopathic proctitis RGO:03871 RGO:03872 gonorrheal proctitis RGO:03872 basaloid carcinoma DOID:7173 RADLEX:RID4281 SNOMEDCT:84570003 RGO:03874 cloacogenic carcinoma RGO:03874 RGO:03876 rectal trauma RGO:03876 RGO:03877 sexual trauma RGO:03877 RGO:03878 iatrogenic trauma RGO:03878 RGO:03879 puerperal trauma RGO:03879 RGO:03880 external trauma RGO:03880 DOID:1993 SNOMEDCT:363351006 RGO:03881 rectal cancer RGO:03881 DOID:4362 RADLEX:RID45683 SNOMEDCT:363354003 RGO:03882 cervical cancer RGO:03882 DOID:119 RGO:03883 vaginal cancer RGO:03883 HP:0005224 ICD10CM:K61.1 SNOMEDCT:91669008 RGO:03884 perirectal abscess RGO:03884 DOID:3247 HP:0002859 ORDO:780 RADLEX:RID4396 SNOMEDCT:302847003 SNOMEDCT:30924005 RGO:03886 rhabdomyosarcoma RGO:03886 RGO:03887 presacral hematoma RGO:03887 RGO:03888 sacral fracture RGO:03888 increased retrorectal space RGO:03889 increased presacral space RGO:03889 RGO:03893 perforated colon RGO:03893 RGO:03894 high-attenuation bile RGO:03894 RADLEX:RID11296 SNOMEDCT:47973001 RGO:03895 artifact RGO:03895 RGO:03896 vicarious excretion of contrast media RGO:03896 SNOMEDCT:66556007 RGO:03897 hematobilia RGO:03897 RGO:03898 inflammatory debris RGO:03898 focal thickening of gallbladder wall RGO:03899 focal gallbladder wall thickening RGO:03899 RGO:03900 adherent gallstone RGO:03900 RGO:03901 adherent sludge RGO:03901 DOID:0050893 RGO:03903 gallbladder adenoma RGO:03903 RGO:03904 gallbladder carcinoid RGO:03904 RGO:03905 gallbladder papilloma RGO:03905 lymph ascites HP:0012281 ICD10CM:I89.8 ORDO:1160 SNOMEDCT:52985009 RGO:03908 chylous ascites RGO:03908 RGO:03910 congenital absence of lymphatic system RGO:03910 RGO:03911 hypoplasia of lymphatic system RGO:03911 benign metastasizing lymphangiomatosis diffuse lymphangioma disseminated lymphangioma disseminated lymphatic malformation lymphatic malformation syndrome RGO:03913 disseminated lymphangiomatosis RGO:03913 ORDO:873 SNOMEDCT:47284001 RGO:03915 desmoid tumor RGO:03915 RGO:03916 pericolic amebic abscess RGO:03916 SNOMEDCT:236011003 RGO:03917 retroperitoneal cyst RGO:03917 SNOMEDCT:387458008 SNOMEDCT:7947003 RGO:03918 aspirin RGO:03918 SNOMEDCT:16403005 RGO:03919 NSAID RGO:03919 alcohol alcoholism DOID:1574 ICD10CM:F10.1 SNOMEDCT:15167005 RGO:03922 alcohol abuse RGO:03922 DOID:8566 SNOMEDCT:88594005 RGO:03923 herpes simplex RGO:03923 RGO:03924 acquired pulsion diverticulum RGO:03924 RGO:03925 traction diverticulum of mid esophagus RGO:03925 RGO:03926 adherent granulomatous lymph node RGO:03926 RGO:03927 esophageal pseudodiverticulosis RGO:03927 SNOMEDCT:276805005 RGO:03928 esophageal leiomyoma RGO:03928 HP:0031021 RADLEX:RID4277 SNOMEDCT:63451008 RGO:03929 squamous papilloma RGO:03929 SNOMEDCT:15970005 RGO:03930 intramural esophageal hematoma RGO:03930 RADLEX:RID3884 RGO:03931 fibrovascular polyp RGO:03931 RADLEX:RID3882 SNOMEDCT:699323007 RGO:03932 inflammatory esophagogastric polyp RGO:03932 RGO:03933 granulomatous lymph node RGO:03933 RGO:03934 localized narrowing of esophagus RGO:03934 HP:0100730 ORDO:2357 SNOMEDCT:9550003 RGO:03935 bronchogenic cyst RGO:03935 SNOMEDCT:24018003 RGO:03936 gastroenteric cyst RGO:03936 RGO:03938 congenital esophageal atresia RGO:03938 RGO:03939 congenital esophageal stenosis RGO:03939 RGO:03940 esophageal leiomyosarcoma RGO:03940 RGO:03941 muscular ring RGO:03941 SNOMEDCT:19898001 RGO:03942 inferior esophageal sphincter RGO:03942 RGO:03943 normal sling fibers of diaphragm RGO:03943 SNOMEDCT:359890009 RGO:03944 fundoplication RGO:03944 RGO:03945 repair of hiatal hernia RGO:03945 RGO:03946 repair of esophageal atresia RGO:03946 RGO:03947 lower esophageal spasm RGO:03947 tracheobronchial rest RGO:03948 cartilaginous ring RGO:03948 RGO:03950 postinstrumentation stricture RGO:03950 RGO:03951 endoscopic perforation RGO:03951 RGO:03952 allergic reaction to nasogastric tube RGO:03952 RGO:03953 resection of retrosternal tumor RGO:03953 SNOMEDCT:254622008 RGO:03957 bronchogenic carcinoma RGO:03957 ORDO:63999 SNOMEDCT:21247003 RGO:03958 mediastinal fibrosis RGO:03958 HP:0002896 RGO:03960 liver tumor RGO:03960 arteriohepatic dysplasia arteriohepatic syndrome DOID:9245 ORDO:52 SNOMEDCT:31742004 RGO:03961 Alagille syndrome RGO:03961 RGO:03965 transverse mucosal folds in the esophagus RGO:03965 nasogastric tube placement RGO:03967 nasogastric intubation RGO:03967 RGO:03968 oral medication RGO:03968 RGO:03969 polyposis of stomach RGO:03969 DOID:11976 ORDO:1267 SNOMEDCT:398565003 SNOMEDCT:414531002 RGO:03971 botulism RGO:03971 DOID:12384 SNOMEDCT:111939009 RGO:03972 dysentery RGO:03972 HP:0030169 ICD10CM:I86.4 SNOMEDCT:91109007 RGO:03973 gastric varices RGO:03973 SNOMEDCT:303082009 RGO:03974 portal hypertensive gastropathy RGO:03974 RGO:03975 drug-related gastritis RGO:03975 RGO:03976 chemotherapy toxicity RGO:03976 DOID:8757 RADLEX:RID3456 SNOMEDCT:60002000 RGO:03977 hypertrophic gastritis RGO:03977 DOID:8680 ICD10CM:K29.2 SNOMEDCT:2043009 RGO:03978 alcoholic gastritis RGO:03978 DOID:4036 RADLEX:RID3451 RGO:03979 Helicobacter pylori gastritis RGO:03979 RADLEX:RID4397 SNOMEDCT:39143003 SNOMEDCT:404082003 RGO:03980 myxoma RGO:03980 RGO:03983 foreign body in lumen RGO:03983 SNOMEDCT:197046003 RGO:03984 gastroduodenal intussusception RGO:03984 RGO:03985 juxtaduodenal abscess RGO:03985 retroperitoneal adenopathy SNOMEDCT:127154008 RGO:03989 retroperitoneal lymphadenopathy RGO:03989 SNOMEDCT:709287005 RGO:03990 gastrointestinal stromal tumor of duodenum RGO:03990 SNOMEDCT:69776003 RGO:03991 acute gastroenteritis RGO:03991 SNOMEDCT:372798009 SNOMEDCT:60978003 RGO:03992 barbiturate RGO:03992 SNOMEDCT:67602004 RGO:03993 acute peritonitis RGO:03993 RGO:03996 bowel necrosis RGO:03996 SNOMEDCT:73761001 RGO:03997 colonoscopy RGO:03997 RGO:03998 catheter jejunostomy RGO:03998 RGO:03999 umbilical artery catheterization RGO:03999 DOID:0050597 RGO:04000 Schistosomiasis japonica RGO:04000 SNOMEDCT:47693006 RGO:04002 perforated appendix RGO:04002 SNOMEDCT:197104005 SNOMEDCT:20464009 RGO:04003 perforated diverticulum RGO:04003 intramural bowel hematoma RGO:04005 intramural bowel hemorrhage RGO:04005 regular small bowel fold thickening RGO:04006 regular thickening of small bowel folds RGO:04006 RGO:04007 Mycobacterium avium-intercellulare RGO:04007 SNOMEDCT:77352002 RGO:04009 shigella RGO:04009 HP:0001732 RGO:04010 pancreatic disease RGO:04010 SNOMEDCT:47563007 SNOMEDCT:70241007 RGO:04011 nutritional deficiency RGO:04011 kwashiorkor syndrome DOID:13579 ICD10CM:E40 SNOMEDCT:58262005 RGO:04012 kwashiorkor RGO:04012 DOID:8457 ORDO:97352 SNOMEDCT:418186002 RGO:04013 pellagra RGO:04013 DOID:10608 SNOMEDCT:396331005 RGO:04014 idiopathic steatorrhea RGO:04014 ICD10CM:A06.4 SNOMEDCT:75119003 RGO:04017 amebic liver abscess RGO:04017 SNOMEDCT:402125000 SNOMEDCT:418453007 RGO:04018 pyogenic abscess RGO:04018 RGO:04019 fungal abscess RGO:04019 cystic HCC RGO:04020 cystic hepatocellular carcinoma RGO:04020 RGO:04021 aortic graft-duodenal fistula RGO:04021 RGO:04022 multiple hypointense liver lesions RGO:04022 RGO:04023 biliary tract perforation RGO:04023 RGO:04024 perforated duodenal diverticulum RGO:04024 RGO:04025 perforated colonic diverticulum RGO:04025 RGO:04026 solid pancreatic mass RGO:04026 RGO:04027 cystic pancreatic mass RGO:04027 DOID:2123 ICD10CM:A21 ORDO:3392 SNOMEDCT:19265001 RGO:04031 tularemia RGO:04031 DOID:4562 SNOMEDCT:73774007 RGO:04032 subacute bacterial endocarditis RGO:04032 RGO:04034 tropical splenic abscess RGO:04034 RGO:04035 subcapsular hematoma RGO:04035 RGO:04036 intrasplenic hematoma RGO:04036 RGO:04037 perisplenic hematoma RGO:04037 DOID:12365 ORDO:673 SNOMEDCT:61462000 RGO:04038 malaria RGO:04038 infarcted spleen DOID:2533 SNOMEDCT:22996003 RGO:04041 splenic infarction RGO:04041 RGO:04043 traumatic fragmentation of spleen RGO:04043 SNOMEDCT:82893001 RGO:04044 splenic atrophy RGO:04044 RGO:04045 diffusely decreased liver intensity RGO:04045 DOID:2725 HP:0005306 RADLEX:RID3972 SNOMEDCT:402867006 SNOMEDCT:83343001 RGO:04046 capillary hemangioma RGO:04046 RGO:04049 extrinsic indentation on duodenum RGO:04049 SNOMEDCT:47977000 RGO:04052 mesenteric hematoma RGO:04052 SNOMEDCT:303086007 RGO:04053 duodenal varices RGO:04053 RGO:04054 retroperitoneal varices RGO:04054 RGO:04055 common bile duct dilatation RGO:04055 DOID:4608 RGO:04056 common bile duct neoplasm RGO:04056 RGO:04057 enlarged abdominal lymph nodes RGO:04057 SNOMEDCT:69559004 RGO:04058 retroperitoneal mass RGO:04058 RADLEX:RID3890 SNOMEDCT:103552005 SNOMEDCT:367643001 SNOMEDCT:441457006 RGO:04060 cyst RGO:04060 RGO:04062 anticholinergic medication RGO:04062 RGO:04063 narcotics RGO:04063 RGO:04064 interstitial emphysema of stomach RGO:04064 RADLEX:RID3459 SNOMEDCT:7399006 RGO:04065 emphysematous gastritis RGO:04065 RGO:04066 recent surgery RGO:04066 SNOMEDCT:53950000 RGO:04067 respiratory therapy RGO:04067 RGO:04068 PEEP RGO:04068 RGO:04069 oxygen tube in esophagus RGO:04069 DOID:2841 HP:0002099 ICD10CM:J45 RADLEX:RID5327 SNOMEDCT:195967001 RGO:04071 asthma RGO:04071 RGO:04072 acid ingestion RGO:04072 SNOMEDCT:387402000 SNOMEDCT:71724000 RGO:04073 ferrous sulfate RGO:04073 DOID:4023 ORDO:36273 RGO:04074 linitis plastica pattern of stomach RGO:04074 RGO:04076 Cryptosporidium gastritis RGO:04076 RGO:04077 hepatic arterial infusion chemotherapy RGO:04077 RGO:04078 acute peptic ulcer with spasm RGO:04078 RGO:04079 chronic peptic ulcer with fibrosis RGO:04079 RGO:04080 extrinsic mass compressing stomach RGO:04080 pancreas cancer pancreatic adenocarcinoma pancreatic carcinoma pancreatic ductal adenocarcinoma DOID:1793 HP:0002894 RADLEX:RID45688 SNOMEDCT:363418001 RGO:04085 pancreatic cancer RGO:04085 SNOMEDCT:312112002 RGO:04087 carcinoma of transverse colon RGO:04087 RGO:04088 deformity of gastric antrum RGO:04088 neutrophil dysfunction RGO:04089 granulomatous disease of infancy RGO:04089 RGO:04091 walled-off peptic ulcer perforation RGO:04091 RGO:04092 prolapsed antral-pyloric fold RGO:04092 RGO:04093 adult pyloric hypertrophy RGO:04093 SNOMEDCT:49209004 RGO:04096 subtotal gastrectomy RGO:04096 RGO:04100 focal acute pancreatitis RGO:04100 HP:0006280 SNOMEDCT:235494005 RGO:04101 chronic pancreatitis RGO:04101 RGO:04102 peripancreatic fluid collection RGO:04102 DOID:3603 RADLEX:RID4164 SNOMEDCT:79143006 RGO:04104 mucinous cystadenocarcinoma RGO:04104 macrocystic adenoma DOID:2633 RADLEX:RID4151 SNOMEDCT:67182003 RGO:04105 mucinous cystadenoma RGO:04105 SNOMEDCT:54164009 RGO:04121 resection of rectosigmoid RGO:04121 RGO:04122 scirrhous RGO:04122 RGO:04123 cloacogenic RGO:04123 DOID:4908 SNOMEDCT:255084004 RGO:04124 anal carcinoma RGO:04124 DOID:3302 HP:0010762 ORDO:178 RADLEX:RID4146 SNOMEDCT:50007008 RGO:04128 chordoma RGO:04128 RGO:04130 extrinsic soft tissue mass RGO:04130 RGO:04133 tail gut cyst RGO:04133 RGO:04147 ischemic enterocolitis preceding onset of renal failure in infants RGO:04147 colon hives RGO:04151 urticaria of colon RGO:04151 RGO:04152 chronic ischemia RGO:04152 colonic obstruction obstruction of colon RGO:04153 colon obstruction RGO:04153 DOID:263 HP:0009726 RGO:04155 kidney cancer RGO:04155 breast carcinoma carcinoma of breast DOID:1612 HP:0003002 RADLEX:RID45682 SNOMEDCT:254837009 RGO:04157 breast cancer RGO:04157 ORDO:300557 SNOMEDCT:254609000 RGO:04159 carcinoma of ampulla of Vater RGO:04159 SNOMEDCT:126880001 RGO:04161 neoplasm of kidney RGO:04161 SNOMEDCT:126838000 RGO:04162 neoplasm of colon RGO:04162 familial polyposis DOID:0050424 ORDO:733 SNOMEDCT:72900001 RGO:04166 familial adenomatous polyposis RGO:04166 RGO:04168 redundant duodenal fold RGO:04168 RGO:04169 flexure defect RGO:04169 RGO:04170 normal papilla of Vater RGO:04170 RGO:04171 peptic ulcer with edema or deformity RGO:04171 acute gastritis DOID:4029 HP:0005263 RADLEX:RID3450 SNOMEDCT:4556007 RGO:04173 gastritis RGO:04173 RGO:04175 anti-inflammatory drug RGO:04175 RGO:04176 suture line ulceration RGO:04176 RGO:04177 bariatric gastric surgery RGO:04177 SNOMEDCT:197012004 RGO:04178 radiation gastritis RGO:04178 SNOMEDCT:95569006 RGO:04180 uremic coma RGO:04180 DOID:12550 SNOMEDCT:72836002 RGO:04181 hepatic coma RGO:04181 RGO:04182 ganglion-blocking agent RGO:04182 RGO:04183 non-obstructive gastric dilatation RGO:04183 RGO:04184 diabetic gastropathy RGO:04184 RGO:04185 acute perigastric inflammation RGO:04185 HP:0030692 SNOMEDCT:254935002 RGO:04186 brain tumor RGO:04186 DOID:1969 HP:0100021 ICD10CM:G80 RADLEX:RID34633 SNOMEDCT:128188000 RGO:04187 cerebral palsy RGO:04187 RGO:04191 traumatic gastric ileus RGO:04191 RGO:04192 spine fracture RGO:04192 SNOMEDCT:40095003 RGO:04193 renal injury RGO:04193 SNOMEDCT:118413007 RGO:04194 body cast RGO:04194 SNOMEDCT:7093002 RGO:04195 renal colic RGO:04195 SNOMEDCT:37389005 RGO:04196 biliary colic RGO:04196 ORDO:330015 RADLEX:RID34657 SNOMEDCT:38342005 RGO:04197 lead poisoning RGO:04197 DOID:6364 HP:0002076 ICD10CM:G43 SNOMEDCT:37796009 RGO:04198 migraine RGO:04198 calculus in ureter ureteral stone RADLEX:RID38587 SNOMEDCT:31054009 RGO:04200 ureteral calculus RGO:04200 SNOMEDCT:61085008 RGO:04201 Taenia saginata RGO:04201 RGO:04202 anisakis with ileocecal phlegmon RGO:04202 SNOMEDCT:17966003 RGO:04203 Taenia solium RGO:04203 RGO:04204 small bowel hamartoma RGO:04204 Peutz-Jeghers disease DOID:3852 ICD10CM:Q85.8 ORDO:2869 SNOMEDCT:54411001 RGO:04205 Peutz-Jeghers syndrome RGO:04205 RGO:04206 malignant small bowel tumor RGO:04206 RGO:04207 benign small bowel tumor RGO:04207 RGO:04208 malignant splenic neoplasm RGO:04208 SNOMEDCT:71911007 RGO:04209 healed infarct RGO:04209 RGO:04210 healed hematoma RGO:04210 RADLEX:RID3953 SNOMEDCT:45647009 RGO:04211 granuloma RGO:04211 Zuckerguss spleen RGO:04214 splenic capsular ascites RGO:04214 SNOMEDCT:12143007 RGO:04216 congenital cyst RGO:04216 RGO:04218 healed abscess RGO:04218 RGO:04219 solitary splenic calcification RGO:04219 RGO:04220 multiple splenic calcifications RGO:04220 RGO:04221 pentastomiasis RGO:04221 RGO:04223 healed Pneumocystis carinii infection RGO:04223 HP:0005206 SNOMEDCT:111374002 RGO:04224 pancreatic pseudocyst RGO:04224 DOID:1793 RGO:04225 pancreatic neoplasm RGO:04225 DOID:12341 SNOMEDCT:307219002 RGO:04226 retroperitoneal sarcoma RGO:04226 RGO:04227 splenic vein obstruction RGO:04227 AAA DOID:7693 HP:0004953 HP:0005112 SNOMEDCT:233985008 RGO:04228 abdominal aortic aneurysm RGO:04228 RGO:04230 diffusely dense spleen RGO:04230 RGO:04231 treated lymphoma RGO:04231 RGO:04232 hypervascular pancreatic lesion RGO:04232 RGO:04235 diffuse peritoneal thickening RGO:04235 RGO:04236 isoechoic liver lesion RGO:04236 oriental cholangiohepatitis RADLEX:RID3389 SNOMEDCT:65001009 RGO:04237 recurrent pyogenic cholangitis RGO:04237 RGO:04239 thickening of bile duct walls RGO:04239 bacterial cholangitis DOID:14270 ICD10CM:K83.0 RADLEX:RID3388 SNOMEDCT:26918003 RGO:04240 ascending cholangitis RGO:04240 wide C-loop wide duodenal C-loop RGO:04242 widening of duodenal C-loop RGO:04242 RGO:04243 abnormal right upper quadrant abdominal gas collection RGO:04243 SNOMEDCT:75100008 RGO:04244 abdominal abscess RGO:04244 RADLEX:RID4803 SNOMEDCT:17204006 RGO:04245 pneumoperitoneum RGO:04245 RGO:04247 subhepatic gas RGO:04247 RGO:04248 perforated duodenal ulcer RGO:04248 RGO:04249 abdominal wall gas RGO:04249 RGO:04250 drainage tube insertion RGO:04250 RGO:04251 iatrogenic pneumoretroperitoneum RGO:04251 RGO:04252 interventional embolization of a viscus RGO:04252 RGO:04253 needle or catheter drainage RGO:04253 RADLEX:RID1745 SNOMEDCT:175905003 RGO:04254 nephrectomy RGO:04254 RGO:04255 retroperitoneal bowel rupture RGO:04255 RGO:04256 retroperitoneal rupture of duodenum RGO:04256 RGO:04257 retroperitoneal rupture of rectum RGO:04257 RGO:04258 abnormal left upper quadrant abdominal gas collection RGO:04258 DOID:2530 HP:0025059 SNOMEDCT:82053000 RGO:04259 splenic abscess RGO:04259 RGO:04261 emphysematous pyelonephritis of left kidney RGO:04261 RGO:04262 pancreatic gas abscess RGO:04262 SNOMEDCT:111368002 RGO:04263 peritoneal fat necrosis RGO:04263 RADLEX:RID1652 SNOMEDCT:234319005 RGO:04265 splenectomy RGO:04265 SNOMEDCT:405563007 RGO:04268 infected pancreatic pseudocyst RGO:04268 RGO:04269 bowel malignancy with perforation RGO:04269 RGO:04270 right anterior pararenal space abscess RGO:04270 SNOMEDCT:270909006 RGO:04271 duodenal perforation RGO:04271 DOID:1724 HP:0002588 ICD10CM:K26 SNOMEDCT:51868009 RGO:04272 duodenal ulcer RGO:04272 RGO:04273 inflamed duodenal diverticulum RGO:04273 RGO:04274 colitis of ascending colon RGO:04274 RGO:04275 ruptured retrocecal appendix RGO:04275 RGO:04276 ruptured retroperitoneal appendix RGO:04276 HP:0025079 SNOMEDCT:69643006 RGO:04277 pancreatic abscess RGO:04277 RGO:04278 decreased abdominal gas in a newborn RGO:04278 RGO:04279 extruded appendicolith RGO:04279 RGO:04280 gallstone extruded into peritoneum RGO:04280 RADLEX:RID5207 SNOMEDCT:244183009 RGO:04281 fluorosis RGO:04281 RGO:04282 abdominal wall scar RGO:04282 RGO:04283 abdominal wall burn RGO:04283 SNOMEDCT:266463007 RGO:04284 psoas abscess RGO:04284 SNOMEDCT:119422004 RGO:04285 mucinous cystadenoma of ovary RGO:04285 GWD dracunculiasis guinea worm disease RGO:04289 guinea worm infection RGO:04289 RGO:04291 focal hyperechoic splenic lesion RGO:04291 ICD10CM:Q89.09 SNOMEDCT:36752001 RGO:04292 congenital splenomegaly RGO:04292 hepatorenal tyrosinemia type 1 tyrosinemia ORDO:882 RGO:04293 tyrosinemia type 1 RGO:04293 DOID:8781 RADLEX:RID34627 SNOMEDCT:36653000 RGO:04297 rubella RGO:04297 disseminated lipogranulomatosis DOID:0050464 SNOMEDCT:79935000 RGO:04298 Farber disease RGO:04298 NOMID chronic infantile neurologic cutaneous articular syndrome neonatal onset multisystem inflammatory disease RGO:04300 infantile multisystem inflammatory disease RGO:04300 CML chronic myelogenous DOID:8552 HP:0005506 ORDO:521 SNOMEDCT:63364005 RGO:04304 chronic myelogenous leukemia RGO:04304 Hurler disease MPS 1-H alpha-L-iduronidase deficiency gargoylism mucopolysaccharidosis type 1-H DOID:12802 ORDO:93473 RADLEX:RID34621 RGO:04306 Hurler syndrome RGO:04306 SNOMEDCT:62065006 RGO:04309 rickettsia RGO:04309 DOID:11256 SNOMEDCT:240613006 RGO:04310 typhus RGO:04310 RGO:04311 mild bowel wall thickening RGO:04311 RGO:04312 marked bowel wall thickening RGO:04312 RGO:04314 early mesenteric infarction RGO:04314 RGO:04315 closed loop bowel obstruction RGO:04315 RGO:04316 armillifer infection of peritoneum RGO:04316 RGO:04317 abdominal wall osteoma RGO:04317 RGO:04318 abdominal wall osteosarcoma RGO:04318 RGO:04319 abdominal wall chondrosarcoma RGO:04319 myositis ossificans progressiva stone man syndrome DOID:13374 ICD10CM:M61.1 ORDO:337 SNOMEDCT:82725007 RGO:04320 fibrodysplasia ossificans progressiva RGO:04320 RGO:04323 congenital abdominal calcifications RGO:04323 RGO:04324 fetal herpes simplex infection RGO:04324 RGO:04325 fetal toxoplasmosis infection RGO:04325 RGO:04326 fetal varicella infection RGO:04326 SNOMEDCT:43258006 RGO:04330 milk-alkali syndrome RGO:04330 RGO:04340 mineral oil granulomas RGO:04340 DOID:12663 ICD10CM:B40 SNOMEDCT:69996000 RGO:04341 blastomycosis RGO:04341 RGO:04342 armillifer infestation RGO:04342 RGO:04345 increased echogenicity of pancreas RGO:04345 RGO:04346 fatty mass in abdomen RGO:04346 appendix epiploica RGO:04347 epiploic appendage of colon RGO:04347 SNOMEDCT:254921004 RGO:04350 angiomyolipoma of kidney RGO:04350 SNOMEDCT:83836003 RGO:04351 omental hernia RGO:04351 SNOMEDCT:72888009 RGO:04352 mesenteric hernia RGO:04352 RADLEX:RID34688 SNOMEDCT:1472023100011910 RGO:04355 epiploic appendagitis RGO:04355 RGO:04358 neuroendocrine tumor of pancreas RGO:04358 RGO:04359 AIDS-related papillitis RGO:04359 RGO:04360 ampullary mass RGO:04360 RGO:04361 calculus in distal common duct RGO:04361 DOID:9965 ICD10CM:B58 SNOMEDCT:187192000 RGO:04362 toxoplasmosis RGO:04362 RGO:04364 cardiac disease RGO:04364 HP:0012050 SNOMEDCT:16740003 SNOMEDCT:442433009 RGO:04365 anasarca RGO:04365 RGO:04366 perforated Meckel diverticulum RGO:04366 RGO:04368 ascites in an infant or child RGO:04368 RGO:04369 surgical complication RGO:04369 RADLEX:RID4764 SNOMEDCT:11108009 RGO:04370 dehiscence RGO:04370 RADLEX:RID1693 SNOMEDCT:301784005 RGO:04371 ileostomy RGO:04371 RADLEX:RID1723 SNOMEDCT:398740003 RGO:04372 colostomy RGO:04372 RADLEX:RID1634 SNOMEDCT:272726003 SNOMEDCT:54956002 RGO:04373 gastrostomy RGO:04373 RADLEX:RID4845 SNOMEDCT:28626004 RGO:04374 colovesical fistula RGO:04374 RGO:04376 duodenal-renal fistula RGO:04376 HP:0100844 SNOMEDCT:25803005 RGO:04380 pancreatic fistula RGO:04380 RGO:04381 ruptured pseudocyst RGO:04381 RGO:04383 external drainage of pseudocyst RGO:04383 RGO:04386 contracted gallbladder RGO:04386 postprandial status RGO:04387 postprandial state RGO:04387 RGO:04394 anomalous position of gallbladder RGO:04394 SNOMEDCT:87541004 RGO:04395 ectopic gallbladder RGO:04395 DOID:758 HP:0001696 ICD10CM:Q89.3 SNOMEDCT:27317008 SNOMEDCT:43876007 RGO:04396 situs inversus RGO:04396 RGO:04400 normal gallbladder folds RGO:04400 RGO:04402 choledochoenteric fistula RGO:04402 RGO:04403 gallstone perforation RGO:04403 RGO:04406 stone in kidney or retrocecal appendix RGO:04406 SNOMEDCT:125273000 RGO:04407 calcified aneurysm RGO:04407 RGO:04408 barium in diverticulum RGO:04408 DOID:1618 RADLEX:RID4285 SNOMEDCT:65877006 RGO:04410 fibroadenoma RGO:04410 DOID:2634 RADLEX:RID4150 SNOMEDCT:47620003 RGO:04411 cystadenoma RGO:04411 DOID:0060072 SNOMEDCT:3898006 RGO:04414 benign neoplasm RGO:04414 malignancies malignancy malignant tumor DOID:162 RADLEX:RID36042 SNOMEDCT:363346000 SNOMEDCT:86049000 RGO:04416 malignant neoplasm RGO:04416 RGO:04417 parasitic granuloma RGO:04417 SNOMEDCT:37763007 RGO:04420 parasite RGO:04420 SNOMEDCT:15956005 RGO:04421 Clonorchis RGO:04421 SNOMEDCT:28291005 RGO:04422 Fasciola RGO:04422 RGO:04423 feces via fistula RGO:04423 RGO:04424 Rh or ABO blood group alloimmunization RGO:04424 RGO:04427 hyperplastic cholecystosis RGO:04427 RGO:04428 ascites with edema of gallbladder wall RGO:04428 HP:0003073 SNOMEDCT:119247004 RGO:04429 hypoalbuminemia RGO:04429 DOID:12351 ICD10CM:K70.1 SNOMEDCT:235875008 RGO:04431 alcoholic hepatitis RGO:04431 RGO:04432 postprandial physiolologic contraction RGO:04432 RGO:04433 incomplete gallbladder distension RGO:04433 RGO:04434 inadequate fasting RGO:04434 RGO:04435 extrahepatic portal vein obstruction RGO:04435 RADLEX:RID39466 SNOMEDCT:300332007 RGO:04438 liver mass RGO:04438 regenerating hepatic nodule regenerative liver nodule RGO:04439 regenerating liver nodule RGO:04439 isolated polycystic liver disease polycystic disease of liver DOID:0050770 DOID:1173 HP:0006557 ORDO:2924 SNOMEDCT:72925005 RGO:04440 polycystic liver disease RGO:04440 RGO:04444 polycystic kidney RGO:04444 SNOMEDCT:91182001 RGO:04448 perforated ulcer RGO:04448 RGO:04449 perforated adenocarcinoma RGO:04449 RGO:04450 Cholangitis In diabetic RGO:04450 RADLEX:RID1674 RGO:04457 sphincterotomy RGO:04457 RGO:04458 biliary-intestinal anastomosis RGO:04458 SNOMEDCT:14687003 RGO:04459 choledochoenterostomy RGO:04459 SNOMEDCT:116241004 RGO:04460 Whipple procedure RGO:04460 RGO:04461 internal or external biliary drainage RGO:04461 RGO:04465 bile duct stricture RGO:04465 RGO:04468 infectious cholangitis RGO:04468 RGO:04469 AIDS-related cholangitis RGO:04469 RGO:04472 parasitic cholangitis RGO:04472 RGO:04473 diverticulum of duodenum RGO:04473 RGO:04474 biliary duct compression RGO:04474 hepatic abscess HP:0100523 RGO:04475 liver abscess RGO:04475 SNOMEDCT:48036004 RGO:04476 pyogenic liver abscess RGO:04476 RGO:04478 fungal liver abscess RGO:04478 RGO:04481 ruptured hydatid cyst RGO:04481 RGO:04483 acute severe biliary obstruction RGO:04483 RGO:04488 bacterial cholangitis with tiny saccular abscesses RGO:04488 SNOMEDCT:255320000 RGO:04490 suppurative RGO:04490 pseudocalculus RGO:04492 contraction of choledochal sphincter RGO:04492 RGO:04494 edema of ampullary segment RGO:04494 RGO:04495 passage of biliary calculus RGO:04495 RGO:04496 extrinsic vascular impression RGO:04496 RADLEX:RID918 SNOMEDCT:244265008 RGO:04497 right hepatic artery RGO:04497 RGO:04498 bile duct varices RGO:04498 RGO:04499 malignant neoplasm of bile duct RGO:04499 RGO:04500 cholangiocarcinoma of gallbladder, ampulla, duodenum, or pancreas RGO:04500 RGO:04501 Klatzkin tumor RGO:04501 RGO:04502 recurrent pyogenic cholangitis with dilated ducts and calculi RGO:04502 RGO:04503 congenital membranous diaphragm of common hepatic duct RGO:04503 RGO:04508 cystic duct insertion RGO:04508 RGO:04511 postoperative plication defect at the site of duct-to-duct anastomosis RGO:04511 RGO:04514 hydatid debris RGO:04514 RGO:04516 impacted stone in Vaterian segment RGO:04516 RGO:04517 papillary edema from recent passage of stone RGO:04517 RGO:04518 papillary stenosis RGO:04518 RGO:04520 surgical injury RGO:04520 DOID:4932 SNOMEDCT:254609000 RGO:04522 ampullary carcinoma RGO:04522 RGO:04523 villous tumor RGO:04523 RGO:04525 duodenal carcinoma RGO:04525 DOID:4948 ORDO:56044 RGO:04526 gallbladder carcinoma RGO:04526 RGO:04532 congenital membranous diaphragm RGO:04532 RGO:04533 advanced hepatocellular disease RGO:04533 RGO:04534 cholangiolytic hepatitis RGO:04534 RGO:04535 lymphadenopathy in porta hepatis RGO:04535 RGO:04537 mucinous Ductectatic Adenocarcinoma of pancreas RGO:04537 RGO:04538 adenomatous polyp of papilla RGO:04538 RGO:04540 chronic perforative cholecystitis RGO:04540 choledochoduodenal fistula RGO:04541 gallstone fistula from gallbladder or bile duct RGO:04541 RGO:04548 granulomatous disease of duodenum or colon RGO:04548 RGO:04549 external or iatrogenic trauma RGO:04549 endoscopic retrograde cholangiopancreatogram endoscopic retrograde cholangiopancreatography SNOMEDCT:386718000 RGO:04550 ERCP RGO:04550 RGO:04558 elevated venous pressure RGO:04558 RGO:04559 tricuspid stenosis or insufficiency RGO:04559 DOID:2043 SNOMEDCT:66071002 RGO:04561 serum hepatitis RGO:04561 DOID:5774 RGO:04565 giant hemangioma RGO:04565 ICD10CM:D56.1 SNOMEDCT:75451007 RGO:04567 thalassemia major RGO:04567 SNOMEDCT:473281000 RGO:04568 obstruction of common bile duct RGO:04568 HP:0002613 SNOMEDCT:1761006 RGO:04569 biliary cirrhosis RGO:04569 SNOMEDCT:243672005 RGO:04570 Echinococcus granulosus RGO:04570 RGO:04571 E. multilocularis RGO:04571 RGO:04572 thrombosis of hepatic vein or upper inferior cava RGO:04572 Pompe disease RGO:04574 glycogen storage disease type 2 RGO:04574 HP:0003774 SNOMEDCT:90688005 RGO:04584 chronic renal failure RGO:04584 SNOMEDCT:60346004 RGO:04589 islet cell carcinoma RGO:04589 DOID:8659 SNOMEDCT:38907003 RGO:04593 varicella RGO:04593 SNOMEDCT:86648009 RGO:04594 Echinococcus multilocularis RGO:04594 RGO:04595 multiple calcified E. granulosus cysts RGO:04595 RGO:04596 multiple healed granulomas RGO:04596 DOID:13450 ICD10CM:B38 ORDO:228123 SNOMEDCT:60826002 RGO:04597 coccidioidomycosis RGO:04597 RGO:04598 severe infection RGO:04598 RGO:04599 multiple healed abscesses RGO:04599 RGO:04601 peritoneal calcifications overlying liver capsule RGO:04601 RGO:04602 ruptured hydrometrocolpos RGO:04602 RGO:04603 primary liver tumor RGO:04603 RGO:04604 thromboemboli in portal vein or IVC RGO:04604 SNOMEDCT:372809001 SNOMEDCT:66261008 RGO:04605 tetracycline RGO:04605 RGO:04609 dilated intrahepatic ducts RGO:04609 DOID:11802 RGO:04613 protein deficiency RGO:04613 RGO:04616 starvation-malnutrition RGO:04616 RGO:04617 fibrosis of liver parenchyma RGO:04617 DOID:2237 HP:0200123 SNOMEDCT:76783007 RGO:04618 chronic hepatitis RGO:04618 RGO:04619 diffuse hepatocellular carcinoma RGO:04619 RGO:04620 E. granulosus cysts RGO:04620 RGO:04621 calcified Echinococcus multilocularis RGO:04621 RADLEX:RID11918 SNOMEDCT:2309006 SNOMEDCT:371256005 RGO:04626 gold RGO:04626 RGO:04628 iron overload of liver RGO:04628 RGO:04629 multiple transfusions RGO:04629 RGO:04631 primary or metastatic diffuse malignancy RGO:04631 SNOMEDCT:76281005 RGO:04632 hepatic congestion RGO:04632 multiple liver cysts HP:0001407 RGO:04633 multiple hepatic cysts RGO:04633 DOID:0060345 SNOMEDCT:58213005 RGO:04635 bacillary angiomatosis RGO:04635 RGO:04637 generalized irregular small bowel folds RGO:04637 RADLEX:RID1627 SNOMEDCT:53442002 RGO:04638 gastrectomy RGO:04638 RADLEX:RID1658 SNOMEDCT:33149006 RGO:04639 pancreatectomy RGO:04639 DOID:1205 HP:0012393 RADLEX:RID39250 SNOMEDCT:408439002 SNOMEDCT:609328004 RGO:04640 allergy RGO:04640 DOID:3118 RGO:04641 hepatobiliary disease RGO:04641 RGO:04642 antimetabolite therapy RGO:04642 RGO:04643 pancreatic non-beta islet cell tumor RGO:04643 SNOMEDCT:55184003 RGO:04644 infectious enteritis RGO:04644 SNOMEDCT:27268008 RGO:04645 Salmonella RGO:04645 RGO:04646 advanced ischemia RGO:04646 SNOMEDCT:107938000 RGO:04651 small bowel resection RGO:04651 DOID:14495 ICD10CM:K91.1 RADLEX:RID5245 SNOMEDCT:80193009 RGO:04653 dumping syndrome RGO:04653 nonobstructive bowel distention nonobstructive distention nonobstructive paralytic ileus paralytic ileus RADLEX:RID5246 SNOMEDCT:55525008 RGO:04656 adynamic ileus RGO:04656 RGO:04658 calcified liver metastasis RGO:04658 RGO:04660 testicular carcinoma RGO:04660 DOID:5605 RGO:04661 medullary carcinoma of breast RGO:04661 DOID:3973 HP:0002865 ORDO:1332 SNOMEDCT:255032005 RGO:04662 medullary thyroid carcinoma RGO:04662 RGO:04663 colloid carcinoma of breast RGO:04663 RGO:04664 colloid carcinoma of thyroid RGO:04664 RGO:04665 mucinous adenocarcinoma of colon RGO:04665 RGO:04666 mucinous adenocarcinoma of stomach RGO:04666 RGO:04667 mucinous adenocarcinoma of pancreas RGO:04667 RGO:04668 liver lesion with central scar RGO:04668 RGO:04674 enteropancreatic fistula RGO:04674 RGO:04675 spontaneous enteropancreatic fistula RGO:04675 RGO:04676 surgical enteropancreatic fistula RGO:04676 RGO:04679 ovarian cancer metastasis RGO:04679 RGO:04680 omental cake RGO:04680 RGO:04683 focal bowel wall thickening RGO:04683 diffusely thick bowel wall diffusely thickened bowel wall RGO:04684 diffuse bowel wall thickening RGO:04684 RGO:04688 cystic abdominal mass in a fetus or newborn RGO:04688 RGO:04690 mesenchymal hepatic hamartoma RGO:04690 HP:0030451 SNOMEDCT:27970007 RGO:04691 mesenteric cyst RGO:04691 RADLEX:RID29522 SNOMEDCT:409614007 RGO:04692 peritoneal fluid RGO:04692 RGO:04693 obstruction of pylorus RGO:04693 HP:0005235 SNOMEDCT:360491009 RGO:04695 jejunal atresia RGO:04695 RGO:04696 jejunal stenosis RGO:04696 RGO:04699 impaired swallowing physiology RGO:04699 RGO:04700 severe prematurity RGO:04700 RGO:04701 depressed swallowing reflex RGO:04701 RGO:04702 impending death RGO:04702 RGO:04703 maternal medication RGO:04703 RGO:04704 gastric suction RGO:04704 RGO:04705 hypoechoic liver RGO:04705 SNOMEDCT:57412004 RGO:04706 acute viral hepatitis RGO:04706 HP:0003774 RGO:04707 end-stage renal disease RGO:04707 RGO:04708 early schistosomiasis RGO:04708 RGO:04709 abdominal calcification in an infant or child RGO:04709 appendiceal fecalith RADLEX:RID4988 RGO:04710 appendicolith RGO:04710 RGO:04712 calculus in Meckel diverticulum RGO:04712 RGO:04713 calculus in urachal cyst RGO:04713 RGO:04714 cysticercosis of abdominal wall RGO:04714 RGO:04715 cysticercosis of back RGO:04715 DOID:271 SNOMEDCT:93469006 RGO:04716 hemangioma of liver RGO:04716 RGO:04717 hamartoma of liver RGO:04717 RGO:04718 perforated hollow viscus in an infant RGO:04718 DOID:10486 HP:0011100 RGO:04719 intestinal atresia RGO:04719 DOID:8445 SNOMEDCT:9707006 RGO:04720 intestinal volvulus RGO:04720 RGO:04721 iatrogenic bowel perforation RGO:04721 RGO:04722 rectal thermometer RGO:04722 SNOMEDCT:439569004 RGO:04723 resuscitation RGO:04723 SNOMEDCT:45460008 RGO:04724 intrauterine transfusion RGO:04724 RGO:04725 umbilical artery thromboembolism RGO:04725 RGO:04726 splenomegaly with normal echogenicity RGO:04726 RGO:04729 early sickle cell disease RGO:04729 SNOMEDCT:37810007 RGO:04730 myelogenous leukemia RGO:04730 RGO:04731 splenomegaly with diffuse hypoechoic pattern RGO:04731 DOID:1040 HP:0005550 SNOMEDCT:51092000 RGO:04732 chronic lymphocytic leukemia RGO:04732 large hyperechoic spleen RGO:04733 splenomegaly with diffuse hyperechoic pattern RGO:04733 RGO:04735 misty mesentery RGO:04735 RGO:04736 mesenteric hemorrhage RGO:04736 RGO:04737 mesenteric inflammation RGO:04737 RGO:04738 mesenteric carcinomatosis RGO:04738 RGO:04739 striations in thickened gallbladder wall RGO:04739 diffuse thickening of gallbladder wall RGO:04740 diffuse gallbladder wall thickening RGO:04740 RGO:04741 increased attenuation of gallbladder lumen RGO:04741 RGO:04742 oral cholecystography RGO:04742 RGO:04743 gallbladder polyp RGO:04743 hepatic neoplasm neoplasm of liver DOID:916 RGO:04744 liver neoplasm RGO:04744 HP:0002027 SNOMEDCT:21522001 RGO:04745 abdominal pain RGO:04745 RGO:04747 acute nonobstructive small bowel distention RGO:04747 SNOMEDCT:267427000 RGO:04751 disaccharidase deficiency RGO:04751 RGO:04757 hyperplastic Peyer patches RGO:04757 RGO:04758 arterial thromboembolism RGO:04758 DOID:0050827 DOID:9814 SNOMEDCT:23685000 RGO:04759 rheumatic heart disease RGO:04759 DOID:0060224 HP:0005110 SNOMEDCT:49436004 RGO:04760 atrial fibrillation RGO:04760 SNOMEDCT:25318002 SNOMEDCT:263884003 RGO:04761 strangulation RGO:04761 RGO:04762 small bowel volvulus RGO:04762 SNOMEDCT:26416006 RGO:04763 drug abuse RGO:04763 DOID:762 HP:0006689 SNOMEDCT:301183007 RGO:04764 bacterial endocarditis RGO:04764 RGO:04766 laryngeal neoplasm RGO:04766 HP:0012163 SNOMEDCT:233988005 RGO:04767 carotid artery aneurysm RGO:04767 innominate artery aneurysm RGO:04768 brachiocephalic artery aneurysm RGO:04768 RGO:04769 buckling of carotid artery RGO:04769 RGO:04770 buckling of brachiocephalic artery RGO:04770 RGO:04772 residual intestinal barium RGO:04772 DOID:2757 RGO:04773 mycobacterial infection RGO:04773 RGO:04775 M. avium-intracellulare RGO:04775 RGO:04776 MAI RGO:04776 RGO:04779 AIDS-related complex RGO:04779 SNOMEDCT:103510000 RGO:04780 Bartonella henselae RGO:04780 RGO:04781 retroperitoneal teratoma RGO:04781 SNOMEDCT:54768000 RGO:04782 distended bladder RGO:04782 RGO:04783 aneurysmal bone cyst of pelvis RGO:04783 RGO:04784 aneurysmal bone cyst of lumbosacral spine RGO:04784 SNOMEDCT:447885009 RGO:04785 sarcoma of pelvis RGO:04785 RGO:04786 sarcoma of lumbosacral spine RGO:04786 DOID:1088 HP:0002435 RADLEX:RID34772 SNOMEDCT:171131006 RGO:04787 meningocele RGO:04787 ICD10CM:E27.49 SNOMEDCT:49111001 RGO:04788 adrenal hemorrhage RGO:04788 SNOMEDCT:237784000 RGO:04789 adrenal cyst RGO:04789 SNOMEDCT:262818004 RGO:04791 splenic hematoma RGO:04791 congenital mesoblastic nephroma mesenchymal renal hamartoma DOID:4772 ORDO:2665 RADLEX:RID4534 SNOMEDCT:11793003 SNOMEDCT:307604008 RGO:04793 mesoblastic nephroma RGO:04793 DOID:3229 RGO:04794 gastric dilatation RGO:04794 RGO:04795 fluid-filled stomach RGO:04795 RGO:04796 fecal masses RGO:04796 RGO:04797 aneurysmal bone cyst of spine RGO:04797 RGO:04798 sarcoma of spine RGO:04798 SNOMEDCT:7102003 RGO:04799 omental cyst RGO:04799 kidney cyst renal cysts DOID:2975 HP:0000107 RADLEX:RID35811 SNOMEDCT:77945009 RGO:04800 renal cyst RGO:04800 HP:0001737 SNOMEDCT:31258000 RGO:04801 pancreatic cyst RGO:04801 RGO:04804 lymphangioma of mesentery RGO:04804 RGO:04805 lymphangioma of omentum RGO:04805 DOID:3605 RGO:04807 ovarian cystadenocarcinoma RGO:04807 RGO:04809 colloid colon carcinoma metastases RGO:04809 RGO:04812 Guinea worm infection of abdominal wall RGO:04812 RGO:04814 liver lesion with T2 hypointense rim RGO:04814 RGO:04815 subacute hematoma RGO:04815 RGO:04816 chronic hematoma RGO:04816 RGO:04817 liver lesions with T1 hypointense rim RGO:04817 RGO:04818 multiple small bowel filling defects RGO:04818 RGO:04819 hypervascular liver metastasis RGO:04819 RGO:04820 hemorrhagic liver metastasis RGO:04820 HP:0030357 ORDO:70573 SNOMEDCT:254632001 RGO:04822 small cell lung cancer RGO:04822 RGO:04823 hypoechoic liver metastasis RGO:04823 RGO:04824 mixed echogenicity liver metastasis RGO:04824 RGO:04825 islet cell carcinoma of pancreas RGO:04825 RGO:04826 anechoic liver lesion RGO:04826 RGO:04827 acute hematoma RGO:04827 SNOMEDCT:25878000 RGO:04828 hepatic artery aneurysm RGO:04828 RGO:04829 portal vein aneurysm RGO:04829 RGO:04830 acquired liver cyst RGO:04830 RGO:04831 traumatic liver cyst RGO:04831 RGO:04832 inflammatory liver cyst RGO:04832 starry sky liver RGO:04833 starry-sky liver RGO:04833 RGO:04835 calcified lymph nodes at porta hepatis RGO:04835 RGO:04836 embolism of lymphangiographic contrast material RGO:04836 HP:0001405 RGO:04837 periportal fibrosis RGO:04837 RGO:04838 hypoechoic liver lesion RGO:04838 RGO:04839 focal sparing in fatty liver RGO:04839 RGO:04840 cystic liver tumor RGO:04840 RGO:04841 complicated hepatic cyst RGO:04841 RGO:04842 upper abdominal mass in a neonate or child RGO:04842 RADLEX:RID4941 SNOMEDCT:289908002 RGO:04844 pregnancy RGO:04844 SNOMEDCT:47753002 RGO:04845 drug-induced esophagitis RGO:04845 SNOMEDCT:420155008 SNOMEDCT:8631001 RGO:04846 potassium chloride RGO:04846 SNOMEDCT:31306009 SNOMEDCT:372697008 RGO:04847 quinidine RGO:04847 SNOMEDCT:43706004 SNOMEDCT:46123006 RGO:04848 ascorbic acid RGO:04848 SNOMEDCT:16624005 RGO:04849 bromide RGO:04849 RGO:04851 patchy liver RGO:04851 RGO:04852 biliary calculi RGO:04852 hepatocellular adenoma HP:0012028 RGO:04853 hepatic adenoma RGO:04853 RGO:04855 calcified pancreatic lesion RGO:04855 RGO:04856 focal chronic pancreatitis RGO:04856 RGO:04858 submucosal hematoma RGO:04858 RGO:04859 small bowel carcinoma RGO:04859 DOID:1520 RGO:04860 colon carcinoma RGO:04860 RGO:04865 infiltrating scirrhous carcinoma RGO:04865 colloid adenocarcinoma DOID:3030 RADLEX:RID4161 SNOMEDCT:72495009 RGO:04866 mucinous adenocarcinoma RGO:04866 RGO:04867 lymphogranuloma venereum colitis RGO:04867 RGO:04868 bowel wall thickening RGO:04868 RADLEX:RID5196 RGO:04869 calcification RGO:04869 RGO:04870 barium in appendix RGO:04870 RGO:04871 barium in diverticula RGO:04871 RGO:04872 air hose injury of rectum RGO:04872 RGO:04875 normal duodenum RGO:04875 RGO:04876 normal colon RGO:04876 RGO:04877 retroperitoneal tumor RGO:04877 RGO:04878 focal shadowing pancreatic lesion RGO:04878 RGO:04879 nonacute hematoma RGO:04879 RGO:04880 congenital obstruction RGO:04880 RADLEX:RID5018 SNOMEDCT:702670001 SNOMEDCT:90293002 RGO:04881 congenital stenosis RGO:04881 SNOMEDCT:76640006 RGO:04882 congenital web RGO:04882 RGO:04883 congenital diaphragm RGO:04883 SNOMEDCT:204731006 RGO:04884 congenital imperforate anus RGO:04884 RGO:04885 congenital meconium plug RGO:04885 RGO:04886 obstructive pulmonary disease RGO:04886 RGO:04887 bullous disease RGO:04887 DOID:6132 HP:0004469 SNOMEDCT:63480004 RGO:04888 chronic bronchitis RGO:04888 SNOMEDCT:86553008 RGO:04891 immunosuppressive therapy RGO:04891 RGO:04892 pyloroduodenal obstruction RGO:04892 RGO:04893 intramural perforation peptic ulcer RGO:04893 RADLEX:RID6260 SNOMEDCT:110418002 RGO:04896 incarcerated hernia RGO:04896 RGO:04900 pelvic neoplasm RGO:04900 fibroid fibroid of uterus leiomyoma of uterus uterine leiomyoma DOID:13223 HP:0000131 RADLEX:RID39270 SNOMEDCT:95315005 RGO:04902 uterine fibroid RGO:04902 contracted cecum RGO:04905 conical cecum RGO:04905 RGO:04907 enema abuse RGO:04907 DOID:3878 HP:0004389 RADLEX:RID5257 RGO:04908 intestinal pseudo-obstruction RGO:04908 HP:0031501 SNOMEDCT:74285003 RGO:04909 pelvic mass RGO:04909 RGO:04915 pelvic surgery RGO:04915 acute colonic pseudo-obstruction RGO:04916 Ogilvie syndrome RGO:04916 RGO:04918 enteric muscle disorder RGO:04918 RGO:04919 chronic strongyloidiasis RGO:04919 SNOMEDCT:281255004 RGO:04920 small bowel obstruction RGO:04920 RGO:04921 appendiceal calculus RGO:04921 RGO:04922 invagination of appendix RGO:04922 ICD10CM:K38.8 SNOMEDCT:91446004 RGO:04923 intussusception of appendix RGO:04923 RGO:04930 fecal mass RGO:04930 RGO:04931 giant type pseudopolyp RGO:04931 RGO:04932 schistosomal granuloma RGO:04932 RGO:04933 ascaris bolus anisakiasis RGO:04933 SNOMEDCT:49293007 RGO:04934 pseudotumor RGO:04934 SNOMEDCT:263757009 RGO:04935 fibrous band RGO:04935 RADLEX:RID33345 SNOMEDCT:63217007 RGO:04937 taeniae coli RGO:04937 RGO:04939 annular lesion of colon RGO:04939 RGO:04940 circular muscle contraction RGO:04940 RGO:04941 pericolic inflammation RGO:04941 HP:0012425 RGO:04942 colon ulcer RGO:04942 RGO:04944 postoperative deformity RGO:04944 RGO:04945 narrow anastomosis RGO:04945 RGO:04948 multiple filling defects in colon RGO:04948 RGO:04949 pseudopolyps RGO:04949 RGO:04950 intraluminal parasites RGO:04950 SNOMEDCT:2572000 RGO:04951 trichuris RGO:04951 SNOMEDCT:281789004 RGO:04955 antibiotic therapy RGO:04955 RADLEX:RID39252 SNOMEDCT:367336001 RGO:04956 chemotherapy RGO:04956 SNOMEDCT:373541007 SNOMEDCT:83532008 RGO:04957 cimetidine RGO:04957 SNOMEDCT:28506006 SNOMEDCT:387155003 RGO:04958 flucytosine RGO:04958 SNOMEDCT:373542000 SNOMEDCT:84078002 RGO:04960 methyldopa RGO:04960 DOID:934 RADLEX:RID34687 SNOMEDCT:34014006 RGO:04962 viral infection RGO:04962 DOID:8536 SNOMEDCT:19551004 SNOMEDCT:4740000 RGO:04963 herpes zoster RGO:04963 SNOMEDCT:417542000 RGO:04964 rotavirus RGO:04964 RGO:04965 staphylococcal colitis RGO:04965 RADLEX:RID3432 SNOMEDCT:449806001 RGO:04966 stercoral colitis RGO:04966 RGO:04967 postoperative colitis RGO:04967 RGO:04968 necrotizing colitis RGO:04968 RGO:04969 symmetric bowel wall thickening RGO:04969 RGO:04970 asymmetric bowel wall thickening RGO:04970 RGO:04971 nondiaphragmatic hernia RGO:04971 HP:0100541 ICD10CM:K41 RADLEX:RID4930 SNOMEDCT:50063009 RGO:04972 femoral hernia RGO:04972 HP:0004872 RADLEX:RID4920 SNOMEDCT:236037000 RGO:04973 incisional hernia RGO:04973 DOID:0060320 HP:0000023 ICD10CM:K40 RADLEX:RID4926 SNOMEDCT:396232000 RGO:04974 inguinal hernia RGO:04974 RADLEX:RID4919 SNOMEDCT:23344004 RGO:04975 lumbar hernia RGO:04975 RGO:04976 paracecal hernia RGO:04976 RADLEX:RID4933 SNOMEDCT:415074004 RGO:04978 perineal hernia RGO:04978 SNOMEDCT:87781009 RGO:04979 retroperitoneal hernia RGO:04979 RADLEX:RID4932 RGO:04980 sciatic hernia RGO:04980 SNOMEDCT:373097002 RGO:04981 pulmonary vein confluence RGO:04981 RGO:04982 extrinsic vascular impression on esophagus RGO:04982 RGO:04983 tortuous thoracic aorta RGO:04983 TAPVC TAPVR total APVC total APVR total anomalous pulmonary venous connection DOID:4297 HP:0005160 ORDO:99125 RADLEX:RID34773 SNOMEDCT:111323005 RGO:04985 total anomalous pulmonary venous return RGO:04985 RGO:04987 infected pulmonary cyst RGO:04987 RGO:04988 infected mediastinal cyst RGO:04988 RGO:04989 infected pulmonary sequestration RGO:04989 RGO:04990 esophageal lung RGO:04990 RGO:04992 esophagobronchial fistula RGO:04992 SNOMEDCT:41279003 RGO:04997 congenital esophagobronchial fistula RGO:04997 RGO:04998 congenital tracheoesophageal fistula RGO:04998 gastric filling defect RGO:05001 filling defect in stomach RGO:05001 RGO:05003 adenomatous polyp of stomach RGO:05003 HP:0002582 ICD10CM:K29.4 SNOMEDCT:84568007 RGO:05004 chronic atrophic gastritis RGO:05004 RADLEX:RID4223 SNOMEDCT:19665009 SNOMEDCT:444408007 RGO:05006 tubular adenoma RGO:05006 hamartoma of stomach RGO:05007 gastric hamartoma RGO:05007 RGO:05011 lung cancer metastasis RGO:05011 granuloma with eosinophils RADLEX:RID3889 SNOMEDCT:63638007 RGO:05014 inflammatory fibroid polyp RGO:05014 SNOMEDCT:35458008 RGO:05015 anisakis RGO:05015 RADLEX:RID4612 SNOMEDCT:66962008 RGO:05018 suture granuloma RGO:05018 SNOMEDCT:72950008 RGO:05019 bile reflux gastritis RGO:05019 RGO:05020 gastrojejunal mucosal prolapse RGO:05020 RADLEX:RID5038 SNOMEDCT:429040005 SNOMEDCT:56208002 RGO:05021 ulcer RGO:05021 RGO:05022 mural inversion RGO:05022 RGO:05023 recurrent gastric carcinoma RGO:05023 RADLEX:RID1629 RGO:05024 gastric stump carcinoma RGO:05024 SNOMEDCT:78809005 RGO:05025 gastric polyp RGO:05025 RGO:05026 hyperplastic gastric polyp RGO:05026 RGO:05027 filling defect in gastric remnant RGO:05027 RGO:05028 lesion of gastric fundus RGO:05028 RGO:05029 giant rugal fold RGO:05029 RADLEX:RID3888 SNOMEDCT:62047007 RGO:05030 hyperplastic polyp RGO:05030 RGO:05031 postsurgical deformity RGO:05031 RADLEX:RID1635 SNOMEDCT:359887003 RGO:05032 Nissen fundoplication RGO:05032 DOID:3717 RGO:05033 gastric adenocarcinoma RGO:05033 RGO:05034 esophageal sqamous cell carcinoma RGO:05034 duodenal obstruction in an infant RADLEX:RID35163 RGO:05035 double bubble sign RGO:05035 HP:0002247 ORDO:1203 SNOMEDCT:51118003 RGO:05037 duodenal atresia RGO:05037 HP:0100867 SNOMEDCT:73120006 RGO:05038 duodenal stenosis RGO:05038 RGO:05040 prolonged bed rest RGO:05040 RGO:05041 loss of abdominal muscle tone RGO:05041 RGO:05042 multiple pregnancies RGO:05042 RGO:05043 small aorticomesenteric vascular angle RGO:05043 old trauma posttraumatic change posttraumatic changes traumatic RADLEX:RID4630 SNOMEDCT:19130008 SNOMEDCT:417746004 RGO:05046 trauma RGO:05046 RGO:05047 severe burn RGO:05047 RGO:05048 tabetic crisis RGO:05048 RGO:05049 anterior abdominal hernia RGO:05049 RADLEX:RID4904 RGO:05050 pericecal hernia RGO:05050 RGO:05051 small bowel mesentery hernia RGO:05051 RGO:05052 sigmoid mesentery hernia RGO:05052 RGO:05053 broad ligament hernia RGO:05053 SNOMEDCT:73962000 RGO:05054 intraperitoneal abscess RGO:05054 SNOMEDCT:235774002 RGO:05055 diverticular abscess RGO:05055 ICD10CM:K65.1 SNOMEDCT:32141002 RGO:05056 mesenteric abscess RGO:05056 RGO:05057 primary intestinal neoplasm RGO:05057 RGO:05058 small bowel carcinoid RGO:05058 HP:0011854 ICD10CM:K66.1 RADLEX:RID34659 SNOMEDCT:45626005 RGO:05059 hemoperitoneum RGO:05059 SNOMEDCT:127144009 RGO:05060 mesenteric lymphadenopathy RGO:05060 solid lesion of mesentery RGO:05064 solid mesenteric lesion RGO:05064 RGO:05066 mesenteric mass RGO:05066 RGO:05068 solid mesenteric mass RGO:05068 RGO:05069 cystic mesenteric lesion RGO:05069 RGO:05070 complicated ascites RGO:05070 RGO:05071 pseudocyst of pancreas invading mesentery RGO:05071 SNOMEDCT:127121006 RGO:05072 cystic lymphadenopathy RGO:05072 RGO:05073 teratoma of testis RGO:05073 RGO:05074 necrotic lymphadenopathy RGO:05074 homogeneously enhancing bowel wall thickening RGO:05075 bowel wall thickening with homogeneous enhancement RGO:05075 heterogeneously enhancing bowel wall thickening RGO:05077 bowel wall thickening with heterogeneous enhancement RGO:05077 RGO:05081 multiple duodenal filling defects RGO:05081 RGO:05083 duodenal polyps RGO:05083 RGO:05086 duodenal wall thickening RGO:05086 RGO:05087 edema of duodenum RGO:05087 RGO:05088 chronic dialysis RGO:05088 RGO:05094 superficial spreading carcinoma RGO:05094 RGO:05095 intramural diverticulosis RGO:05095 RGO:05096 hirsute esophagus RGO:05096 RGO:05097 mesenteric artery collaterals RGO:05097 RGO:05098 celiac artery collaterals RGO:05098 carcinoma of stomach DOID:10534 HP:0012126 ORDO:63443 RADLEX:RID34623 SNOMEDCT:363349007 RGO:05099 gastric cancer RGO:05099 DOID:219 HP:0003003 RGO:05100 colon cancer RGO:05100 gastric wall thickening thick gastric folds thick gastric wall thickened gastric folds RGO:05101 gastric fold thickening RGO:05101 RGO:05105 decreased fold pattern in duodenum and small bowel RGO:05105 RGO:05106 cancer of right kidney RGO:05106 DOID:3121 RGO:05107 gallbladder cancer RGO:05107 RGO:05108 para-aortic lymphadenopathy RGO:05108 postbulbar duodenal ulceration SNOMEDCT:78054007 RGO:05109 postbulbar duodenal ulcer RGO:05109 RGO:05110 postbulbar duodenal scar RGO:05110 RADLEX:RID1524 SNOMEDCT:181614006 SNOMEDCT:5798000 RGO:05111 diaphragm RGO:05111 SNOMEDCT:297165008 RGO:05112 duodenal web RGO:05112 SNOMEDCT:197171003 RGO:05114 bacterial peritonitis RGO:05114 SNOMEDCT:309088003 RGO:05116 renal mass RGO:05116 DOID:5151 HP:0009732 RADLEX:RID4466 SNOMEDCT:403818001 SNOMEDCT:41252002 RGO:05118 plexiform neurofibroma RGO:05118 SNOMEDCT:72884006 RGO:05122 vascular shunt RGO:05122 RGO:05123 splenorenal shunt RGO:05123 SNOMEDCT:20767001 RGO:05124 portocaval shunt RGO:05124 RGO:05125 lacerated vessel RGO:05125 RGO:05126 transected vessel RGO:05126 DOID:864 RADLEX:RID3699 SNOMEDCT:61599003 RGO:05128 phlebitis RGO:05128 ICD10CM:K75.1 SNOMEDCT:85514005 RGO:05129 pylephlebitis RGO:05129 RGO:05130 hypertrophied uterine vessels RGO:05130 RGO:05131 compression of iliac vein RGO:05131 RGO:05132 anomalous pulmonary vein draining below the diaphragm RGO:05132 SNOMEDCT:239937004 RGO:05136 idiopathic aortitis RGO:05136 RGO:05137 necrotizing angiitis from drug abuse RGO:05137 RGO:05138 mycotic aneurysms RGO:05138 RGO:05140 vascular cuffing RGO:05140 SNOMEDCT:13018008 RGO:05141 neovascularity RGO:05141 RGO:05142 vascular displacement RGO:05142 DOID:519 RADLEX:RID3684 SNOMEDCT:70933002 RGO:05144 aortitis RGO:05144 RGO:05145 microaneurysms RGO:05145 RGO:05147 portal venous obstruction RGO:05147 SNOMEDCT:56073001 RGO:05148 collateral circulation RGO:05148 RGO:05149 artery of Drummond RGO:05149 RADLEX:RID38008 RGO:05150 arc of Riolan RGO:05150 RGO:05151 meandering mesenteric artery RGO:05151 HP:0100545 SNOMEDCT:68109007 RGO:05152 arterial stenosis RGO:05152 DOID:1712 HP:0001650 RADLEX:RID34590 SNOMEDCT:60573004 RGO:05154 aortic stenosis RGO:05154 RGO:05155 aortic occlusion RGO:05155 RGO:05156 anomalous origin of vessel RGO:05156 RGO:05158 congenital absence of vessel RGO:05158 carcinoma of lung DOID:1324 HP:0100526 RADLEX:RID45686 SNOMEDCT:93880001 RGO:05159 lung cancer RGO:05159 DOID:3462 SNOMEDCT:27391005 RGO:05160 hamartomatous polyp RGO:05160 RGO:05161 early small bowel carcinoma RGO:05161 RGO:05162 atypical carcinoma RGO:05162 RGO:05163 solitary small bowel mass with preserved mucosa RGO:05163 RGO:05164 polyposis syndrome RGO:05164 SNOMEDCT:79501007 RGO:05166 tapeworm RGO:05166 RGO:05167 hyperplastic Peyer patches in ileum RGO:05167 RGO:05168 metastatic lung cancer RGO:05168 RGO:05169 metastatic ovarian cancer RGO:05169 RGO:05170 large adjacent neoplasm RGO:05170 pregnant uterus SNOMEDCT:9258009 RGO:05171 gravid uterus RGO:05171 RGO:05174 healed abdomnial abscess RGO:05174 RGO:05175 healed retroperitoneal abscess RGO:05175 RGO:05176 healed psoas abscess RGO:05176 RGO:05177 normal pelvic veins RGO:05177 RGO:05178 splenolith RGO:05178 DOID:12337 HP:0012871 ICD10CM:I86.1 RADLEX:RID39184 SNOMEDCT:51070004 RGO:05180 varicocele RGO:05180 RGO:05181 lympholith RGO:05181 RGO:05183 hepatolith RGO:05183 RGO:05185 colonic diverticulum calculus RGO:05185 RGO:05186 duodenal diverticulum calculus RGO:05186 RGO:05187 Meckel diverticulum calculus RGO:05187 RGO:05188 enteroliths in small bowel RGO:05188 RGO:05189 enteroliths in Meckel diverticulum RGO:05189 RGO:05190 renal calculi in calyceal diverticulum RGO:05190 RGO:05191 renal calculi in hydronephrosis RGO:05191 RGO:05192 thrombosis of portal vein RGO:05192 RGO:05197 sonographic bulls-eye sign RGO:05197 RGO:05198 milk of calcium in gallbladder RGO:05198 RGO:05199 milk of calcium in kidney RGO:05199 SNOMEDCT:446123007 RGO:05200 tuberculous abscess RGO:05200 RGO:05201 chronic tubo-ovarian abscess RGO:05201 RGO:05202 layering abdominal calcifications RGO:05202 endometrioma in scar RGO:05203 scar endometrioma RGO:05203 RGO:05205 extrinsic deformity of gallbladder RGO:05205 DOID:1168 RGO:05207 familial hyperlipidemia RGO:05207 SNOMEDCT:248435007 RGO:05208 prolonged fever RGO:05208 ICD10CM:T73.0 SNOMEDCT:212968006 RGO:05209 starvation RGO:05209 RGO:05214 healed Echinococcus granulosus cyst RGO:05214 RGO:05217 metastatic colon cancer RGO:05217 RGO:05218 metastatic kidney cancer RGO:05218 RGO:05220 multifocal acute intrahepatic hemorrhage RGO:05220 RGO:05224 choledochal cyst type I RGO:05224 RGO:05225 gallbladder wall varices RGO:05225 biliary ductal dilatation RGO:05226 dilated bile ducts RGO:05226 SNOMEDCT:82821008 RGO:05228 extrahepatic biliary atresia RGO:05228 RGO:05229 biliary duct web RGO:05229 RGO:05230 biliary duct diaphragm RGO:05230 RGO:05233 periportal lymphadenopathy RGO:05233 RGO:05235 metastatic carcinoma of liver RGO:05235 RGO:05237 metastatic carcinoma of stomach RGO:05237 RGO:05238 metastatic carcinoma of pancreas RGO:05238 dense liver high-attenuation liver RGO:05239 hyperdense liver RGO:05239 RGO:05242 neonatal chylous ascites RGO:05242 RGO:05243 nephrotic syndrome with hypoproteinemia RGO:05243 urinary ascites urinary outlet obstruction with rupture SNOMEDCT:26170003 RGO:05245 urine ascites RGO:05245 RGO:05250 polycystic liver RGO:05250 SNOMEDCT:89056007 RGO:05253 cavernous lymphangioma RGO:05253 RGO:05254 colon wall thickening RGO:05254 RGO:05256 treated hepatocellular carcinoma RGO:05256 RGO:05257 healed liver abscess RGO:05257 calcific liver lesion calcified liver lesion RGO:05258 liver lesion with calcification RGO:05258 RGO:05261 biliary tract calculus RGO:05261 RGO:05262 old hematoma RGO:05262 RGO:05266 calcified portal vein thrombus RGO:05266 hepar lobatum RGO:05269 hepatic gumma RGO:05269 RGO:05270 calcified hepatic artery RGO:05270 liver granuloma ICD10CM:D86.89 SNOMEDCT:714253009 RGO:05271 hepatic granuloma RGO:05271 RGO:05273 treated melanoma RGO:05273 RGO:05275 microcolon in newborn RGO:05275 HP:0010448 ORDO:1198 SNOMEDCT:37054000 RGO:05276 colonic atresia RGO:05276 RGO:05278 meconium plug in newborn RGO:05278 SNOMEDCT:441850003 RGO:05279 appendiceal stump RGO:05279 RGO:05280 appendiceal mass RGO:05280 SNOMEDCT:255825000 RGO:05281 cytotoxin RGO:05281 RGO:05284 congenital gallbladder hypoplasia RGO:05284 SNOMEDCT:300345006 RGO:05285 small gallbladder RGO:05285 RGO:05286 congenital intestinal malrotation RGO:05286 HP:0001748 SNOMEDCT:10362008 RGO:05288 polysplenia RGO:05288 RGO:05289 innumerable tiny nodules in small bowel or colon RGO:05289 RGO:05290 multiple splenic hypointensities RGO:05290 RGO:05291 pyogenic abscesses RGO:05291 RGO:05292 fungal microabscesses RGO:05292 RGO:05293 candida microabscesses RGO:05293 RGO:05294 congenital splenic cyst RGO:05294 RGO:05295 traumatic splenic pseudocyst RGO:05295 RGO:05296 normal stomach RGO:05296 RADLEX:RID96 SNOMEDCT:25271004 RGO:05297 normal gastroesophageal junction RGO:05297 RGO:05298 gastric outlet RGO:05298 RGO:05299 malignant neoplasm with thickening of bowel wall RGO:05299 RGO:05300 metastasis to serosa RGO:05300 RGO:05302 inflammatory bowel disease with wall thickening RGO:05302 RGO:05303 armillifer infestation of peritoneum RGO:05303 RGO:05304 armillifer infestation of mesentery RGO:05304 RGO:05305 meconium in lumen RGO:05305 RGO:05306 meconium in peritoneum RGO:05306 RGO:05307 meconium in intestinal wall RGO:05307 RGO:05308 lung carcinoma metastasis RGO:05308 RGO:05309 metastasis from carcinoma of breast RGO:05309 RGO:05311 metastasis from carcinoma of colon RGO:05311 RGO:05313 focal cystic or low density splenic lesion RGO:05313 RGO:05314 lymphadenopathy at splenic hilum RGO:05314 RGO:05315 multiple splenic hyperintensities RGO:05315 RGO:05316 anomalous origin of splenic artery RGO:05316 RGO:05317 anomalous origin of celiac artery RGO:05317 RGO:05319 splenic artery fibromuscular hyperplasia RGO:05319 RGO:05320 splenic artery stenosis RGO:05320 RGO:05321 splenic artery occlusion RGO:05321 RGO:05322 thromboembolism of portal vein RGO:05322 RGO:05323 thromboembolism of splenic vein RGO:05323 SPEN RADLEX:RID4173 SNOMEDCT:27078002 RGO:05325 solid and papillary epithelial neoplasm RGO:05325 RGO:05327 metastasis from kidney carcinoma RGO:05327 RGO:05328 metastasis from lung carcinoma RGO:05328 RGO:05329 metastasis from stomach carcinoma RGO:05329 RGO:05330 metastasis from gallbladder carcinoma RGO:05330 RGO:05331 lymphadenopathy in celiac axis RGO:05331 RGO:05333 congenital cysts RGO:05333 RGO:05334 adult polycystic kidney disease RGO:05334 RGO:05339 pseudoaneurysm of splenic artery RGO:05339 RGO:05340 cystic metastasis RGO:05340 RGO:05342 hepatoma metastasis RGO:05342 metastasis from melanoma RGO:05344 melanoma metastasis RGO:05344 RGO:05345 breast carcinoma metastasis RGO:05345 RGO:05346 ovary carcinoma metastasis RGO:05346 RGO:05347 cystic islet cell tumor RGO:05347 RGO:05348 cystic insulinoma RGO:05348 RGO:05349 duct ectatic mucinous adenocarcinoma RGO:05349 RGO:05350 papillary intraductal adenocarcinoma RGO:05350 RGO:05351 anaplastic adenocarcinoma RGO:05351 RGO:05352 pancreatic duct dilatation RGO:05352 RGO:05353 pancreatic duct ectasia RGO:05353 SNOMEDCT:235973002 RGO:05354 pancreatic duct obstruction RGO:05354 RGO:05355 complex pancreatic lesion RGO:05355 DOID:3111 RADLEX:RID4153 SNOMEDCT:21008007 RGO:05356 cystadenocarcinoma RGO:05356 RGO:05358 pancreatic duct stenosis RGO:05358 RGO:05359 nutritional RGO:05359 RGO:05360 pancreatitis due to biliary disease RGO:05360 RGO:05361 gallstone in common duct RGO:05361 RGO:05365 metastasis from mucinous adenocarcinoma of colon RGO:05365 RGO:05366 intraparenchymal hemorrhage RGO:05366 RGO:05367 old abscess RGO:05367 pancreatic lesion characterized by hemorrhage RGO:05368 pancreatic lesion characterized by blood RGO:05368 SNOMEDCT:33997006 RGO:05370 aneurysm of gastroduodenal artery RGO:05370 SNOMEDCT:57614009 RGO:05371 aneurysm of pancreaticoduodenal artery RGO:05371 RGO:05372 pseudoaneurysm of hepatic artery RGO:05372 RGO:05373 pseudoaneurysm of gastroduodenal artery RGO:05373 RGO:05374 pseudoaneurysm pancreaticoduodenal artery RGO:05374 RGO:05376 metastasis from angiosarcoma RGO:05376 RGO:05377 metastasis from leiomyosarcoma RGO:05377 RGO:05378 metastasis from carcinoid RGO:05378 RGO:05379 metastasis from renal cell carcinoma RGO:05379 RGO:05380 metastasis from adrenal carcinoma RGO:05380 RGO:05381 metastasis from thyroid carcinoma RGO:05381 RGO:05386 carcinoma of ampulla RGO:05386 DOID:6785 ORDO:83469 SNOMEDCT:128735004 RGO:05387 desmoplastic small round cell tumor RGO:05387 SNOMEDCT:45187003 RGO:05388 mesenteric fibromatosis RGO:05388 DOID:2334 RGO:05389 metastatic carcinoma RGO:05389 RGO:05390 practolol peritonitis RGO:05390 RGO:05392 splenic artery encasement RGO:05392 RGO:05393 vascular splenic mass RGO:05393 RGO:05394 hemangiosarcoma of spleen RGO:05394 RGO:05395 metastasis from colloid carcinoma RGO:05395 RGO:05396 metastasis from papillary cystadenocarcinoma of ovary RGO:05396 DOID:0060123 SNOMEDCT:387837005 RGO:05397 neoplasm of soft tissues RGO:05397 osteomas HP:0100246 RADLEX:RID4002 SNOMEDCT:302858007 SNOMEDCT:83612000 RGO:05398 osteoma RGO:05398 RGO:05399 implantation by malignant neoplasm RGO:05399 RGO:05400 invasion by malignant neoplasm RGO:05400 RGO:05401 protein-losing gastroenteropathy RGO:05401 RGO:05402 metastatic disease in lymphatics RGO:05402 SNOMEDCT:92260003 RGO:05403 benign ovarian tumor RGO:05403 RGO:05404 candida abscess RGO:05404 RGO:05405 Pneumocystis carinii abscess RGO:05405 SNOMEDCT:191394000 RGO:05406 calcified lymph nodes RGO:05406 RGO:05409 pancreatic duct stricture or filling defect with normal parenchyma RGO:05409 RGO:05410 pancreatic duct stricture or filling defect with abnormal parenchyma RGO:05410 RGO:05412 pancreatic duct hyperplasia RGO:05412 RGO:05413 inflammatory lymph nodes RGO:05413 RGO:05415 web in inferior vena cava RGO:05415 HP:0001004 RGO:05418 lymphatic obstruction RGO:05418 mesothelioma of peritoneum DOID:1788 HP:0100003 RGO:05421 peritoneal mesothelioma RGO:05421 RGO:05424 mesenteric mesothelioma RGO:05424 RGO:05425 chronic right heart failure RGO:05425 IVC thrombosis inferior vena cava thrombosis thrombosis of IVC SNOMEDCT:281595001 RGO:05426 thrombosis of inferior vena cava RGO:05426 RGO:05428 thromboembolism of hepatic veins RGO:05428 SNOMEDCT:95598005 RGO:05429 ruptured ovarian cyst RGO:05429 RGO:05430 idiopathic dilatation of colon RGO:05430 DOID:3876 RGO:05431 colonic pseudo-obstruction RGO:05431 RGO:05432 megacolon with rupture RGO:05432 RGO:05433 ulcerating bowel disease RGO:05433 SNOMEDCT:50257008 RGO:05434 perforation of colon RGO:05434 SNOMEDCT:241164003 RGO:05436 air contrast barium enema RGO:05436 RGO:05437 immunosuppressive therapy in renal transplant patient RGO:05437 RGO:05438 pneumothorax via congenital pleuroperitoneal fistula RGO:05438 RGO:05439 vaginal aspiration RGO:05439 RGO:05440 douching RGO:05440 RGO:05441 sudden squatting RGO:05441 RGO:05442 oral sex RGO:05442 RGO:05443 postpartum exercises RGO:05443 RGO:05445 Rubin test RGO:05445 RADLEX:RID50156 SNOMEDCT:10847001 RGO:05446 bronchoscopy RGO:05446 RGO:05447 diagnostic pneumoperitoneum RGO:05447 DOID:9675 HP:0002097 SNOMEDCT:87433001 RGO:05448 pulmonary emphysema RGO:05448 RGO:05449 ruptured bulla RGO:05449 RGO:05450 lesser sac gas RGO:05450 RGO:05451 giant Meckel diverticulum RGO:05451 RGO:05452 infected fibroid RGO:05452 RGO:05453 obstructed hiatal hernia RGO:05453 SNOMEDCT:196903009 RGO:05454 obstructed diaphragmatic hernia RGO:05454 SNOMEDCT:236042008 RGO:05455 obstructed internal hernia RGO:05455 RGO:05456 obstructed external hernia RGO:05456 RGO:05457 giant colonic diverticulum RGO:05457 RGO:05459 pyloric obstruction from ulcer RGO:05459 RGO:05460 pyloric obstruction from neoplasm RGO:05460 RGO:05461 ruptured hydrometrocolpos with plastic peritonitis RGO:05461 RGO:05462 old hematoma in liver RGO:05462 RGO:05463 old hematoma in spleen RGO:05463 RGO:05464 old hematoma in retroperitoneum RGO:05464 RGO:05465 metastatic calcinosis RGO:05465 ICD10CM:D73.4 SNOMEDCT:79040006 RGO:05467 cyst of spleen RGO:05467 SNOMEDCT:77945009 RGO:05468 cyst of kidney RGO:05468 ICD10CM:K86.2 SNOMEDCT:31258000 RGO:05469 cyst of pancreas RGO:05469 SNOMEDCT:79883001 RGO:05470 cyst of ovary RGO:05470 RGO:05471 histoplasmosis in liver RGO:05471 RGO:05472 tuberculosis in liver RGO:05472 RGO:05473 histoplasmosis in spleen RGO:05473 RGO:05474 histoplasmosis in lymph node RGO:05474 RGO:05475 histoplasmosis in peritoneum RGO:05475 RGO:05476 tuberculosis in spleen RGO:05476 RGO:05477 tuberculosis in lymph node RGO:05477 RGO:05478 tuberculosis in peritoneum RGO:05478 RGO:05479 bile duct filling defect RGO:05479 DOID:3255 SNOMEDCT:14269005 SNOMEDCT:404052009 SNOMEDCT:405943005 RGO:05480 sarcoma botryoides RGO:05480 GI fistula GI tract fistula RGO:05481 gastrointestinal tract fistula RGO:05481 echogenic liver RGO:05484 hyperechoic liver RGO:05484 RGO:05485 diffuse infiltrating liver metastasis RGO:05485 RGO:05486 cystic liver lesion RGO:05486 embryonal sarcoma SNOMEDCT:128734000 RGO:05487 undifferentiated sarcoma RGO:05487 RGO:05489 cystic liver metastasis RGO:05489 RGO:05490 cystadenocarcinoma of uterus RGO:05490 RGO:05491 fatty liver lesion RGO:05491 RGO:05492 bile duct narrowing or obstruction RGO:05492 RGO:05493 hyperechoic liver lesion RGO:05493 RGO:05494 bowel rupture RGO:05494 RGO:05495 ruptured gallbladder empyema RGO:05495 RGO:05496 perforated GI tract neoplasm RGO:05496 RGO:05498 ascaris perforation of intestine RGO:05498 SNOMEDCT:396559007 RGO:05499 necrotic tumor RGO:05499 RGO:05501 dilated stomach RGO:05501 HP:0100668 RGO:05502 bowel duplication RGO:05502 RGO:05503 bowel atresia RGO:05503 RGO:05504 fixed gallbladder filling defect RGO:05504 HP:0006278 SNOMEDCT:264304000 RGO:05505 ectopic pancreatic tissue RGO:05505 SNOMEDCT:70450006 RGO:05506 ectopic gastric tissue RGO:05506 SNOMEDCT:76235005 RGO:05507 pseudopolyp RGO:05507 SNOMEDCT:232001 RGO:05508 congenital fold RGO:05508 RGO:05509 solid liver lesion in an infant or young child RGO:05509 SNOMEDCT:443144000 RGO:05510 metastatic sarcoma RGO:05510 RGO:05511 solid liver lesion in adult RGO:05511 RGO:05512 solid liver lesion in an older child or adolescent RGO:05512 embryonal liver sarcoma RGO:05513 undifferentiated liver sarcoma RGO:05513 RGO:05514 mixed mesenchymal liver sarcoma RGO:05514 DOID:3254 RGO:05515 bile duct rhabdomyosarcoma RGO:05515 RGO:05517 lower abdominal mass in a neonate or child RGO:05517 RGO:05518 gastrointestinal tract thumbprinting RGO:05518 RGO:05519 mural metastasis RGO:05519 GI tract bulls-eye lesion RGO:05520 bulls-eye lesion of gastrointestinal tract RGO:05520 RGO:05521 malabsorption pattern in small bowel RGO:05521 RGO:05522 congenital biliary tract abnormality RGO:05522 RGO:05523 idiopathic perforation of common bile duct RGO:05523 RGO:05524 diverticulum of common bile duct RGO:05524 RGO:05525 benign mesenchymal tumor RGO:05525 RGO:05526 echoes within bile ducts RGO:05526 RGO:05528 food particles via reflux RGO:05528 RGO:05529 diffuse hepatic calcifications RGO:05529 DOID:13738 SNOMEDCT:17890003 RGO:05530 hepatic infarction RGO:05530 RGO:05531 hepatic ischemia RGO:05531 RGO:05533 biliary-pleural fistula RGO:05533 RGO:05534 congenital biliary-pleural fistula RGO:05534 RGO:05536 hemorrhagic liver lesion RGO:05536 RGO:05539 alkaloid ingestion RGO:05539 RGO:05540 bush tea disease RGO:05540 RGO:05541 infection of liver RGO:05541 DOID:13564 ICD10CM:B44 ORDO:1163 RADLEX:RID34591 SNOMEDCT:65553006 RGO:05542 aspergillosis RGO:05542 DOID:4905 SNOMEDCT:372142002 RGO:05543 carcinoma of pancreas RGO:05543 RADLEX:RID45711 SNOMEDCT:45211000 RGO:05545 catheterization RGO:05545 RGO:05546 vena cavography RGO:05546 SNOMEDCT:94381002 RGO:05547 hepatic metastasis RGO:05547 RGO:05548 septic peritonitis with gas-forming organism RGO:05548 RGO:05549 blunt abdominal trauma RGO:05549 ICD10CM:T86.41 SNOMEDCT:235911006 RGO:05550 liver transplant rejection RGO:05550 RGO:05551 focal hypodense liver lesion RGO:05551 RADLEX:RID4734 SNOMEDCT:312608009 SNOMEDCT:35933005 RGO:05552 laceration RGO:05552 focal fatty change of liver focal hepatic steatosis RGO:05553 focal fatty infiltration of liver RGO:05553 RGO:05555 cryptococcus microabscesses RGO:05555 RGO:05557 annular abdominal calcification RGO:05557 RGO:05561 dampened waveform of hepatic vein RGO:05561 RGO:05562 liver lesion with fluid-fluid level RGO:05562 RGO:05563 hemorrhagic hepatic cyst RGO:05563 RGO:05564 infected hepatic cyst RGO:05564 RGO:05565 hemorrhagic hepatocellular adenoma RGO:05565 RGO:05566 giant cavernous hemangioma RGO:05566 RGO:05567 liver lesion with contrast fill-in RGO:05567 RGO:05568 extrinsic pressure from normal or enlarged liver RGO:05568 RGO:05569 extrinsic pressure from normal or enlarged spleen RGO:05569 RGO:05570 extrinsic pressure from normal or enlarged splenic flexure of colon RGO:05570 RGO:05571 extrinsic pressure from normal or enlarged left kidney RGO:05571 RGO:05572 extrinsic pressure from normal or enlarged heart RGO:05572 RGO:05573 extrinsic pressure from normal or enlarged aortic aneurysm RGO:05573 RGO:05574 extragastric malignancy RGO:05574 RGO:05578 carcinoma of splenic flexure of colon RGO:05578 RGO:05579 carcinoma of liver RGO:05579 DOID:4451 RGO:05580 carcinoma of kidney RGO:05580 SNOMEDCT:9429009 RGO:05582 gastroplasty RGO:05582 RGO:05583 antral diaphragm RGO:05583 RGO:05584 antral web RGO:05584 RGO:05585 prolapsed antral mucosa RGO:05585 RGO:05586 prolapsed antral polyp RGO:05586 RGO:05588 prepyloric scarring RGO:05588 RGO:05589 prepyloric inflammation RGO:05589 RGO:05590 prepyloric stricture RGO:05590 RGO:05591 extrinsic compression from pancreatic lesion RGO:05591 RGO:05592 extrinsic compression from renal lesion RGO:05592 RGO:05593 extrinsic compression from retroperitoneal lesion RGO:05593 RGO:05594 extrinsic compression from colonic lesion RGO:05594 RGO:05595 extrinsic compression from duodenal lesion RGO:05595 RGO:05596 carcinoma of gastric antrum RGO:05596 SNOMEDCT:326072005 RGO:05598 carcinoma of head of pancreas RGO:05598 RGO:05599 retained sponge RGO:05599 RGO:05600 trauma with gastric perforation RGO:05600 RGO:05601 trauma with duodenal perforation RGO:05601 RGO:05602 trauma with colonic perforation RGO:05602 DOID:3918 RGO:05603 pancreatic cystadenoma RGO:05603 RGO:05605 carcinoma of adrenal gland RGO:05605 RGO:05606 adenoma of adrenal gland RGO:05606 SNOMEDCT:237783006 RGO:05608 adrenal mass RGO:05608 RGO:05611 gastrointestinal stromal tumor of posterior wall of stomach RGO:05611 SNOMEDCT:95548009 RGO:05612 retroperitoneal edema RGO:05612 RGO:05613 retroperitoneal cellulitis RGO:05613 RGO:05614 urinary leakage RGO:05614 RGO:05615 herniation of omentum RGO:05615 DOID:10534 RGO:05616 gastric neoplasm RGO:05616 DOID:5280 HP:0031025 RGO:05617 gastric leiomyosarcoma RGO:05617 SNOMEDCT:372140005 RGO:05618 carcinoma of gallbladder RGO:05618 RGO:05619 Courvoisier gallbladder RGO:05619 RGO:05621 colon lesion RGO:05621 SNOMEDCT:312114001 RGO:05622 carcinoma of hepatic flexure RGO:05622 RGO:05623 amebic pericolic abscess RGO:05623 RGO:05624 duodenal diverticulitis with giant duodenal diverticulum RGO:05624 RGO:05625 duodenal abscess with giant duodenal diverticulum RGO:05625 SNOMEDCT:126824007 RGO:05626 neoplasm of stomach RGO:05626 RGO:05627 omental mass RGO:05627 DOID:3890 ORDO:79276 SNOMEDCT:234422006 RGO:05628 acute intermittent porphyria RGO:05628 RGO:05629 multiple carcinomas RGO:05629 TOA tuboovarian abscess tubovarian abscess RADLEX:RID3712 SNOMEDCT:58949002 RGO:05630 tubo-ovarian abscess RGO:05630 RGO:05631 cecal diaphragm RGO:05631 RGO:05632 cecal web RGO:05632 RGO:05633 cecal adhesion RGO:05633 RGO:05634 sacrococcygeal lesion RGO:05634 RGO:05636 lymphoma of rectum RGO:05636 RGO:05637 lymphoma of retrorectal soft tissues RGO:05637 HP:0004871 SNOMEDCT:284077005 RGO:05640 perineal fistula RGO:05640 RGO:05641 pelvic fistula RGO:05641 gallbladder nonvisualization nonvisualized gallbladder ICD10CM:R93.2 SNOMEDCT:224405004 RGO:05642 nonvisualization of gallbladder RGO:05642 SNOMEDCT:41587001 RGO:05646 last trimester of pregnancy RGO:05646 RGO:05647 stone in cystic duct remnant RGO:05647 RGO:05648 stone in common duct RGO:05648 RGO:05649 nonshadowing lesion in the gallbladder RGO:05649 RGO:05650 ectopic pancreatic mucosa RGO:05650 RGO:05651 echo within gallbladder RGO:05651 RGO:05652 gallstone or gallbladder sludge in a fetus or neonate RGO:05652 RGO:05654 recent passage of gallstone from gallbladder or common duct RGO:05654 RGO:05655 biliary-enteric fistula to duodenum or colon RGO:05655 RGO:05656 postbulbar duodenal ulcer adjacent to ampulla with spasm or fibrosis RGO:05656 RGO:05657 papillitis or fibrosis of ampulla of Vater RGO:05657 RGO:05658 mucin-producing cholangiocarcinoma RGO:05658 SNOMEDCT:126858004 RGO:05659 neoplasm of ampulla of Vater RGO:05659 RGO:05661 neoplasm of major bile duct RGO:05661 RGO:05662 penetrating duodenal ulcer RGO:05662 SNOMEDCT:126857009 RGO:05663 neoplasm of common bile duct RGO:05663 RGO:05664 sclerosing cholangitis with prestenotic saccular outpouchings RGO:05664 RGO:05665 complicated Caroli disease RGO:05665 SNOMEDCT:85057007 RGO:05666 liver cyst RGO:05666 RGO:05668 traumatic stricture RGO:05668 RGO:05669 iatrogenic biliary stricture RGO:05669 DOID:5039 RGO:05670 myoblastoma RGO:05670 RGO:05671 metastasis from carcinoma of stomach RGO:05671 RGO:05672 pancreas cancer metastasis RGO:05672 RGO:05673 metastasis from carcinoma of gallbladder RGO:05673 DOID:3121 ICD10CM:C23 RGO:05675 malignant neoplasm of gallbladder RGO:05675 ICD10CM:C25 RGO:05676 malignant neoplasm of pancreas RGO:05676 DOID:10155 SNOMEDCT:363508008 RGO:05677 malignant neoplasm of intestine RGO:05677 RGO:05680 upside-down stomach RGO:05680 RGO:05682 embedded gallstone RGO:05682 RGO:05683 hyperechoic focus in gallbladder wall RGO:05683 RGO:05684 external penetrating trauma RGO:05684 RGO:05685 gas in gallbladder or biliary tract RGO:05685 RGO:05686 incompetent sphincter of Oddi RGO:05686 RGO:05687 calcified portal vein RGO:05687 RADLEX:RID1552 SNOMEDCT:49909006 RGO:05688 mucus RGO:05688 RGO:05696 multiple endocrine neoplasia syndrome 2B RGO:05696 large gallbladder RGO:05698 enlarged gallbladder RGO:05698 RGO:05699 gallbladder empyema RGO:05699 hydrops of gallbladder RGO:05700 gallbladder hydrops RGO:05700 gallbladder agenesis ICD10CM:Q44.0 SNOMEDCT:86507001 RGO:05703 congenital absence of gallbladder RGO:05703 gallbladder hypoplasia SNOMEDCT:93259002 RGO:05704 congenital hypoplasia of gallbladder RGO:05704 RGO:05707 lobar or segmental liver perfusion abnormality RGO:05707 RGO:05708 subsegmental liver perfusion abnormality RGO:05708 hepatic perfusion abnormality perfusion abnormality of liver RGO:05709 liver perfusion abnormality RGO:05709 RGO:05710 portal vein ligation RGO:05710 SNOMEDCT:235763006 RGO:05711 traumatic proctitis RGO:05711 RGO:05712 chemical proctitis RGO:05712 SNOMEDCT:35324004 SNOMEDCT:387190006 RGO:05713 paraldehyde RGO:05713 heterotaxia heterotaxia syndrome heterotaxy situs ambiguous DOID:0050545 ORDO:157769 SNOMEDCT:14821001 RGO:05714 situs ambiguus RGO:05714 SNOMEDCT:30873000 RGO:05718 esophageal fistula RGO:05718 hypodense liver low-density liver RGO:05720 low-attenuation liver RGO:05720 RGO:05722 multiple solid liver lesions RGO:05722 DOID:169 SNOMEDCT:255046005 RGO:05727 neuroendocrine tumor RGO:05727 RGO:05728 drug-induced liver toxicity RGO:05728 SNOMEDCT:30427009 SNOMEDCT:372694001 RGO:05729 erythromycin RGO:05729 SNOMEDCT:387220006 SNOMEDCT:40556005 RGO:05730 diphenylhydantoin RGO:05730 RGO:05731 regenerating or dysplastic nodules RGO:05731 RGO:05735 teratoid tumor RGO:05735 ORDO:213504 RGO:05736 adenocarcinoma of ovary RGO:05736 RGO:05739 pseudomucinous cystadenocarcinoma of ovary RGO:05739 RGO:05741 central necrosis of any malignant lesion RGO:05741 RGO:05743 mucin-secreting liver metastasis RGO:05743 RGO:05746 avascular or hypovascular liver lesion RGO:05746 DOID:3953 RGO:05749 adrenal neoplasm RGO:05749 DOID:1115 HP:0100242 RADLEX:RID4521 SNOMEDCT:2424003 SNOMEDCT:424413001 RGO:05751 sarcoma RGO:05751 RGO:05754 focal fatty sparing RGO:05754 RGO:05755 hypervascular liver lesion RGO:05755 RGO:05759 carcinoma of stomach or uterus RGO:05759 RGO:05760 cystadenocarcinoma of ovary or pancreas RGO:05760 RGO:05761 bronchogenic squamous cell carcinoma RGO:05761 RGO:05763 carcinoma of the breast RGO:05763 RGO:05765 carcinoma of the colon RGO:05765 RGO:05766 carcinoma of the lung RGO:05766 RGO:05767 carcinoma of the stomach RGO:05767 RGO:05768 carcinoma of the ovary RGO:05768 RGO:05769 carcinoma of the pancreas RGO:05769 SNOMEDCT:48391002 RGO:05772 calcified granuloma RGO:05772 RGO:05776 parasites in bile ducts RGO:05776 RGO:05788 hypoenhancing liver lesion RGO:05788 RGO:05791 hypoenhancing liver metastasis RGO:05791 RGO:05794 splenic arteriovenous fistula RGO:05794 SNOMEDCT:6838000 RGO:05795 mesenteric arteriovenous fistula RGO:05795 RGO:05796 hepatic arterioportal fistula RGO:05796 RGO:05800 long-term oral estrogen therapy RGO:05800 RGO:05801 infantile hemangioendothelioma of liver RGO:05801 RGO:05804 right upper lobectomy RGO:05804 RGO:05805 left upper lobectomy RGO:05805 RGO:05820 liver lesions with no circumferential rim on MR RGO:05820 RGO:05822 focal fatty deposit in liver RGO:05822 RGO:05823 surgical liver defect packed with omental fat RGO:05823 RGO:05825 acute hepatic hematoma RGO:05825 RGO:05826 normal signal intensity liver surrounded by low signal intensity liver RGO:05826 RGO:05827 cirrhosis with regenerating nodules RGO:05827 RGO:05828 hepatic edema RGO:05828 RGO:05829 high T1 signal intensity liver lesion RGO:05829 RGO:05830 extrinsic compression or invasion by carcinoma of pancreas or stomach RGO:05830 RGO:05831 lymphadenopathy of porta hepatis RGO:05831 PNH DOID:0060284 HP:0004818 ORDO:447 SNOMEDCT:1963002 RGO:05836 paroxysmal nocturnal hemoglobinuria RGO:05836 RADLEX:RID1595 RGO:05837 TIPS RGO:05837 RGO:05838 umbilical venous catheterization RGO:05838 RGO:05839 estrogen therapy RGO:05839 SNOMEDCT:85514005 RGO:05840 portal phlebitis RGO:05840 RGO:05841 pancreatic disease with portal obstruction RGO:05841 RGO:05843 catheterization of umbilical or mesenteric artery or vein RGO:05843 RGO:05844 percutaneous abscess drainage RGO:05844 RGO:05846 hepatic artery embolization RGO:05846 RGO:05848 mechanical bowel obstruction with ischemia RGO:05848 RGO:05850 increased periportal signal intensity on MR RGO:05850 metastasis to spleen RGO:05852 splenic metastasis RGO:05852 DOID:2394 HP:0100615 RADLEX:RID45687 SNOMEDCT:363443007 RGO:05854 ovarian cancer RGO:05854 RADLEX:RID4164 RGO:05865 mucinous cystic neoplasm RGO:05865 RADLEX:RID3374 SNOMEDCT:12393003 RGO:05867 peliosis RGO:05867 WDHA syndrome pancreatic cholera syndrome watery diarrhea - hypokalemia - achlorhydria syndrome DOID:6977 SNOMEDCT:39998009 RGO:05868 Verner-Morrison syndrome RGO:05868 DOID:0080177 ICD10CM:K76.5 ORDO:890 SNOMEDCT:65617004 RGO:05875 hepatic veno-occlusive disease RGO:05875 RGO:05876 liver lesion and elevated alpha fetoprotein RGO:05876 RGO:05882 cystic liver neoplasm RGO:05882 RGO:05883 necrotic liver neoplasm RGO:05883 nonfasting patient RGO:05886 nonfasting state RGO:05886 THAD RGO:05887 transient hepatic attenuation difference RGO:05887 RGO:05895 colonoscopy in inflammatory bowel disease RGO:05895 RGO:05896 air-contrast barium enema in inflammatory bowel disease RGO:05896 SNOMEDCT:129129003 RGO:05898 infectious peritonitis RGO:05898 RGO:05901 renal cancer metastasis RGO:05901 RADLEX:RID5425 SNOMEDCT:125670008 SNOMEDCT:19227008 RGO:05903 foreign body RGO:05903 RGO:05905 bowel gas RGO:05905 hepatization of gallbladder RGO:05907 sludge-filled gallbladder RGO:05907 RADLEX:RID35441 SNOMEDCT:22845004 RGO:05909 phrygian cap RGO:05909 multiseptate gallbladder RGO:05910 septated gallbladder RGO:05910 DOID:234 RGO:05915 colon adenocarcinoma RGO:05915 RADLEX:RID1546 SNOMEDCT:39477002 RGO:05916 feces RGO:05916 RADLEX:RID187 SNOMEDCT:181269000 SNOMEDCT:28231008 RGO:05926 gallbladder RGO:05926 RGO:05941 infiltrative liver metastasis RGO:05941 DOID:10534 HP:0012126 RADLEX:RID34623 RGO:05942 stomach cancer RGO:05942 RGO:05944 necrotic liver tumor RGO:05944 RGO:05945 liver biopsy RGO:05945 RGO:05946 liver tumor embolization RGO:05946 RADLEX:RID5576 SNOMEDCT:19923001 RGO:05947 catheter RGO:05947 DOID:13768 ICD10CM:B66.0 SNOMEDCT:1059007 RGO:05962 opisthorchiasis RGO:05962 RGO:05963 bulls-eye liver metastasis RGO:05963 mucocele of appendix RADLEX:RID34731 RGO:05964 appendiceal mucocele RGO:05964 perforation of gut RGO:05965 bowel perforation RGO:05965 DOID:3756 HP:0005543 ICD10CM:D68.59 ORDO:745 SNOMEDCT:76407009 RGO:05966 protein C deficiency RGO:05966 DOID:2451 HP:0004855 ICD10CM:D68.59 ORDO:743 SNOMEDCT:1563006 RGO:05967 protein S deficiency RGO:05967 SNOMEDCT:274504000 RGO:05969 umbilical vessel catheterization RGO:05969 RGO:05970 mesenteric vessel catheterization RGO:05970 SNOMEDCT:173830003 RGO:05971 gastric lavage RGO:05971 RGO:05972 cirrhosis with portal hypertension RGO:05972 HP:0001824 SNOMEDCT:89362005 RGO:05973 weight loss RGO:05973 RGO:05975 retroperitoneal gas RGO:05975 RGO:05976 extraperitoneal gas RGO:05976 RGO:05977 chronic bowel obstruction RGO:05977 RGO:05979 congenital small bowel stenosis RGO:05979 SNOMEDCT:16376000 RGO:05980 congenital duodenal stenosis RGO:05980 SNOMEDCT:39476006 RGO:05981 congenital rectal stenosis RGO:05981 RGO:05982 aortic pseudoaneurysm RGO:05982 RGO:05983 gastroduodenal artery pseudoaneurysm RGO:05983 RGO:05984 gastroduodenal artery aneurysm RGO:05984 RGO:05985 pancreaticoduodenal artery pseudoaneurysm RGO:05985 RGO:05986 pancreaticoduodenal artery aneurysm RGO:05986 RGO:05987 splenic artery pseudoaneurysm RGO:05987 RGO:05989 vascular compression of pancreatic duct RGO:05989 RGO:05990 pancreatic duct stricture or filling defect RGO:05990 RGO:05991 Ascaris in pancreatic duct RGO:05991 DOID:1781 RADLEX:RID45691 SNOMEDCT:363478007 RGO:05992 thyroid cancer RGO:05992 S. japonica RGO:05994 Schistosoma japonica RGO:05994 RGO:05995 hyperechoic liver metastasis RGO:05995 RGO:06007 ampullary cancer RGO:06007 DOID:10021 HP:0006771 SNOMEDCT:363403002 RGO:06008 duodenal cancer RGO:06008 DOID:4927 ORDO:99978 SNOMEDCT:253017000 SNOMEDCT:6492006 RGO:06009 Klatskin tumor RGO:06009 RGO:06013 kidney tumor RGO:06013 RGO:06015 recent bowel surgery RGO:06015 RGO:06034 ingestion of sharp foreign body RGO:06034 HP:0005203 RADLEX:RID4945 SNOMEDCT:19995004 RGO:06036 Boerhaave syndrome RGO:06036 RGO:06038 hepatic artery chemotherapy RGO:06038 RGO:06039 esophageal wall invasion from adjacent malignancy RGO:06039 RGO:06040 metastasis to esophagus RGO:06040 DOID:1105 RGO:06041 esophageal metastasis RGO:06041 RGO:06043 inverted appendiceal stump RGO:06043 RGO:06044 surgical deformity RGO:06044 RGO:06046 surgical anastomosis RGO:06046 RGO:06051 scirrhous colon adenocarcinoma RGO:06051 RGO:06052 mucinous colon adenocarcinoma RGO:06052 RGO:06062 calcium bilirubinate gallstone RGO:06062 RGO:06063 calcium carbonate gallstone RGO:06063 craniostenosis RGO:06064 premature craniosynostosis RGO:06064 vitamin D intoxication DOID:9971 ICD10CM:E67.3 SNOMEDCT:27712000 RGO:06069 hypervitaminosis D RGO:06069 RGO:06081 congenital premature craniosynostosis RGO:06081 RGO:06089 fetal rubella syndrome RGO:06089 acro-cranial-facial syndrome acro-cranio-facial syndrome acrocraniofacial dysostosis RGO:06094 acro-cranio-facial dysostosis RGO:06094 ORDO:1908 RGO:06096 aminopterin fetopathy RGO:06096 DOID:0050462 ORDO:83 SNOMEDCT:62964007 RGO:06097 Antley-Bixler syndrome RGO:06097 DOID:14737 ORDO:1520 SNOMEDCT:715421009 RGO:06101 craniofrontonasal dysplasia RGO:06101 ORDO:1528 SNOMEDCT:715422002 RGO:06102 craniotelencephalic dysplasia RGO:06102 microcrania DOID:10907 HP:0000252 ICD10CM:Q02 SNOMEDCT:1829003 RGO:06113 microcephaly RGO:06113 HP:0002084 ICD10CM:Q01 SNOMEDCT:55999004 RGO:06118 encephalocele RGO:06118 Cervenka syndrome Pepper syndrome ORDO:193 SNOMEDCT:56604005 RGO:06127 Cohen syndrome RGO:06127 HP:0010541 SNOMEDCT:51603000 RGO:06128 cutis verticis gyrata RGO:06128 psychosocial dwarfism RGO:06129 deprivation dwarfism RGO:06129 DOID:14796 ICD10CM:Q87.1 ORDO:235 SNOMEDCT:2593002 RGO:06130 Dubowitz syndrome RGO:06130 Fraser-François syndrome Ullrich-Feichtiger syndrome cryptophthalmia syndrome DOID:0090001 ORDO:2052 SNOMEDCT:204102004 RGO:06135 Fraser syndrome RGO:06135 ORDO:568 SNOMEDCT:438504004 RGO:06145 Lenz microphthalmia syndrome RGO:06145 ORDO:2461 RGO:06149 Marden-Walker syndrome RGO:06149 DOID:9281 SNOMEDCT:297225000 RGO:06151 maternal phenylketonuria RGO:06151 SNOMEDCT:389197004 RGO:06153 microcephalic osteodysplastic dysplasia RGO:06153 RGO:06154 microcephaly-lymphedema syndrome RGO:06154 RGO:06158 prenatal radiation RGO:06158 SNOMEDCT:205650008 RGO:06163 trisomy 9 RGO:06163 SNOMEDCT:205655003 RGO:06164 trisomy 22 RGO:06164 49,XXXXX syndrome chromosome XXXXX syndrome penta X pentasomy X SNOMEDCT:43248007 RGO:06165 XXXXX syndrome RGO:06165 HP:0002410 RGO:06173 aqueduct stenosis RGO:06173 DOID:2626 HP:0200022 ORDO:2807 RADLEX:RID4086 SNOMEDCT:18021007 RGO:06175 choroid plexus papilloma RGO:06175 RGO:06176 expansion of middle fossa RGO:06176 DOID:4626 HP:0002324 ICD10CM:Q04.3 ORDO:2177 SNOMEDCT:30023002 RGO:06177 hydranencephaly RGO:06177 porencephaly HP:0002132 SNOMEDCT:65705009 RGO:06181 porencephalic cyst RGO:06181 HP:0030713 ORDO:1053 RGO:06184 vein of Galen aneurysm RGO:06184 congenital macrocrania congenital megalencephaly HP:0004488 RGO:06185 congenital macrocephaly RGO:06185 DOID:9250 ORDO:36 SNOMEDCT:715951007 RGO:06190 acrocallosal syndrome RGO:06190 RGO:06191 aminoacidurias RGO:06191 DOID:0080032 ORDO:1513 SNOMEDCT:205506004 RGO:06194 craniodiaphyseal dysplasia RGO:06194 DOID:14261 ICD10CM:Q99.2 ORDO:908 SNOMEDCT:613003 RGO:06200 fragile X syndrome RGO:06200 DOID:14761 ORDO:380 SNOMEDCT:32985001 RGO:06202 Greig cephalopolysyndactyly syndrome RGO:06202 RGO:06208 leukodystrophies RGO:06208 dysplastic gangliocytoma of cerebellum HP:0500009 ORDO:65285 RADLEX:RID4506 SNOMEDCT:67944007 RGO:06209 Lhermitte-Duclos disease RGO:06209 DOID:0050858 ORDO:561 SNOMEDCT:73284007 RGO:06211 Marshall-Smith syndrome RGO:06211 DOID:0060886 ORDO:2780 SNOMEDCT:254129003 RGO:06213 osteopathia striata with cranial sclerosis RGO:06213 DOID:2446 SNOMEDCT:86073008 RGO:06214 pituitary gigantism RGO:06214 RGO:06217 Schwarz-Lélek syndrome RGO:06217 DOID:0060251 ORDO:3152 SNOMEDCT:17568006 RGO:06218 sclerosteosis RGO:06218 Russell-Silver syndrome Silver syndrome congenital hemiatrophy DOID:14681 ORDO:813 RGO:06219 Silver-Russell syndrome RGO:06219 Weaver-Smith syndrome DOID:14731 ICD10CM:Q87.3 ORDO:3447 SNOMEDCT:63119004 RGO:06222 Weaver syndrome RGO:06222 RGO:06224 abnormal contour of calvarium RGO:06224 DOID:0080049 SNOMEDCT:279082008 RGO:06233 acromesomelic dysplasia RGO:06233 DOID:4445 HP:0100702 ICD10CM:G93.0 ORDO:2356 RADLEX:RID3891 SNOMEDCT:33595009 RGO:06234 arachnoid cyst RGO:06234 RGO:06236 craniopagus twins RGO:06236 RGO:06237 hemimegancephaly RGO:06237 RGO:06244 unilateral small cranium RGO:06244 HP:0005469 RGO:06251 flat occiput RGO:06251 peripheral dysostosis DOID:14669 ORDO:950 SNOMEDCT:66758006 RGO:06256 acrodysostosis RGO:06256 HP:0000269 RGO:06260 prominent occiput RGO:06260 RGO:06263 occipital cephalohematoma RGO:06263 DOID:4997 HP:0100252 SNOMEDCT:34643004 RGO:06264 diaphyseal dysplasia RGO:06264 MUscle-LIver-BRain-EYe nanism Perheentupa syndrome DOID:0050436 ORDO:2576 RGO:06267 Mulibrey nanism RGO:06267 ORDO:669 SNOMEDCT:42432003 RGO:06268 otopalatodigital syndrome RGO:06268 prominent central forehead HP:0002007 SNOMEDCT:90145001 RGO:06269 frontal bossing RGO:06269 DOID:0080043 ICD10CM:Q77.0 ORDO:932 SNOMEDCT:2391001 RGO:06272 achondrogenesis RGO:06272 DOID:3783 ORDO:192 SNOMEDCT:15182000 RGO:06274 Coffin-Lowry syndrome RGO:06274 oculocerebrorenal syndrome DOID:1056 SNOMEDCT:79385002 RGO:06281 Lowe syndrome RGO:06281 HP:0000242 RGO:06292 biparietal bossing RGO:06292 RGO:06295 localized bulge of the calvarium or scalp RGO:06295 HP:0012541 SNOMEDCT:83095000 RGO:06297 cephalohematoma RGO:06297 RGO:06299 arachnoid cyst with erosion RGO:06299 DOID:0080031 ICD10CM:M27.8 RADLEX:RID3738 SNOMEDCT:254145001 RGO:06301 fibrous dysplasia RGO:06301 DOID:4445 RGO:06303 leptomeningeal cyst RGO:06303 DOID:3565 HP:0002858 ORDO:2495 RADLEX:RID4088 SNOMEDCT:19453003 RGO:06304 meningioma RGO:06304 RGO:06307 Paget disease with secondary malignancy RGO:06307 hypoplasia of skull base RGO:06309 skull base hypoplasia RGO:06309 HP:0012366 RGO:06317 basilar invagination RGO:06317 RGO:06318 congenital craniovertebral junction anomaly RGO:06318 RGO:06325 occipital craniotomy in a child RGO:06325 thickening of skull vault with basilar invagination RGO:06330 tam-o-shanter skull RGO:06330 RGO:06333 focally dense calvarium RGO:06333 RGO:06342 arteriovenous malformation of dura RGO:06342 Feuerstein-Mins syndrome Schimmelpenning-Feuerstein syndrome Solomon syndrome linear sebaceous nevus sequence nevus sebaceous of Jadassohn organoid nevus syndrome ORDO:35125 SNOMEDCT:239112008 RGO:06346 epidermal nevus syndrome RGO:06346 DOID:0060098 HP:0011846 ORDO:58040 RADLEX:RID4006 SNOMEDCT:55333008 RGO:06351 osteoblastoma RGO:06351 osteocartilaginous exostosis HP:0030431 RADLEX:RID4136 SNOMEDCT:443093007 SNOMEDCT:52299001 RGO:06352 osteochondroma RGO:06352 RGO:06355 diffusely dense calvarium RGO:06355 DOID:2340 HP:0001363 ICD10CM:Q75.0 RADLEX:RID34603 SNOMEDCT:57219006 RGO:06368 craniosynostosis RGO:06368 RGO:06376 dense or thick skull RGO:06376 primary hypertrophic osteoarthropathy ICD10CM:M89.4 ORDO:2796 RGO:06383 pachydermoperiostosis RGO:06383 ORDO:916 RGO:06385 Aase-Smith syndrome RGO:06385 ORDO:1782 SNOMEDCT:254123002 RGO:06388 dysosteosclerosis RGO:06388 DOID:4253 ORDO:2485 RADLEX:RID34660 SNOMEDCT:44697002 RGO:06390 melorheostosis RGO:06390 ORDO:2671 SNOMEDCT:77817004 RGO:06391 Neu-Laxova syndrome RGO:06391 ORDO:309334 SNOMEDCT:87074006 RGO:06396 Salla disease RGO:06396 RGO:06398 trichodentoosseous dysplasia RGO:06398 RGO:06399 Troell-Junet syndrome RGO:06399 RGO:06401 focally dense skull base RGO:06401 RGO:06412 diffusely dense skull base RGO:06412 RGO:06421 localized skull thinning RGO:06421 RGO:06422 parietal thinning RGO:06422 RGO:06423 congenital arachnoid cyst RGO:06423 RGO:06426 localized temporal horn hydrocephalus RGO:06426 RGO:06429 generalized skull thinning RGO:06429 RGO:06430 long-standing hydrocephalus RGO:06430 RGO:06435 diffuse demineralization of skull RGO:06435 RGO:06449 erosion of inner table of skull RGO:06449 SNOMEDCT:20682003 RGO:06451 pacchionian granulation RGO:06451 RGO:06452 arteriovenous malformation of brain surface RGO:06452 RGO:06453 cisterna magna anomaly RGO:06453 RADLEX:RID3907 RGO:06454 epidermoid RGO:06454 SNOMEDCT:50751005 RGO:06458 sinus pericranii RGO:06458 RGO:06459 button sequestrum of skull RGO:06459 RGO:06465 fibrosing osteitis RGO:06465 RGO:06467 solitary osteolytic skull lesion RGO:06467 RGO:06479 button sequestrum RGO:06479 DOID:6312 SNOMEDCT:446939001 RGO:06481 chordoma of clivus RGO:06481 RGO:06482 dermal sinus RGO:06482 RGO:06494 radiolucent skull lesion RGO:06494 RGO:06496 congenital fibromatosis RGO:06496 RGO:06497 ectopic intradiploic glial tissue RGO:06497 RADLEX:RID6218 SNOMEDCT:272681004 RGO:06500 fontanelle RGO:06500 RGO:06501 frontal fenestra RGO:06501 parietal foramina isolated DOID:0060285 HP:0002697 ORDO:60015 SNOMEDCT:29307005 RGO:06505 parietal foramina RGO:06505 ABC HP:0012063 ICD10CM:M85.5 SNOMEDCT:203468000 SNOMEDCT:76000001 RGO:06517 aneurysmal bone cyst RGO:06517 RGO:06519 chondroid lesion RGO:06519 HP:0003001 SNOMEDCT:32037004 RGO:06521 glomus jugulare tumor RGO:06521 RGO:06523 intracranial tumor with erosion RGO:06523 RGO:06528 neurofibroma of bone or scalp RGO:06528 RGO:06532 hemophilic pseudotumor RGO:06532 RGO:06535 intradiploic neural heterotopia RGO:06535 RGO:06542 genetic dwarfism RGO:06542 RGO:06543 radiation therapy in childhood RGO:06543 Simmonds disease postpartum pituitary necrosis DOID:9476 ORDO:91355 SNOMEDCT:237684005 RGO:06544 Sheehan syndrome RGO:06544 HP:0002680 RGO:06546 J-shaped sella turcica RGO:06546 RGO:06549 optic chiasm glioma RGO:06549 RGO:06552 anterior extension of pituitary tumor RGO:06552 RGO:06554 suprasellar tumor RGO:06554 stretched sella HP:0005463 RGO:06555 elongated sella turcica RGO:06555 RGO:06557 enlarging head RGO:06557 scooped sella RGO:06558 omega sella RGO:06558 RGO:06563 dysplastic sella turcica RGO:06563 RGO:06564 enlargement or erosion of sella turcica RGO:06564 DOID:3840 HP:0030062 ORDO:54595 RADLEX:RID4147 SNOMEDCT:189179009 SNOMEDCT:40009002 RGO:06566 craniopharyngioma RGO:06566 DOID:12016 RGO:06576 frontal lobe neoplasm RGO:06576 RGO:06582 mucocele of sphenoid sinus RGO:06582 Turmschädel acrocephaly high-head syndrome hypsicephaly oxycephalia steeple head tower skull HP:0000263 ICD10CM:Q75.0 RADLEX:RID5416 SNOMEDCT:48069004 RGO:06587 oxycephaly RGO:06587 RADLEX:RID3935 RGO:06591 Rathke cleft cyst RGO:06591 RGO:06592 erosion of sphenoid wing RGO:06592 RGO:06597 parasellar aneurysm of internal carotid artery RGO:06597 RGO:06599 erosion of the petrous ridge, pyramid, or apex RGO:06599 acoustic neurinoma acoustic neuroma RADLEX:RID4481 SNOMEDCT:126949007 RGO:06600 acoustic schwannoma RGO:06600 RADLEX:RID3398 SNOMEDCT:40487009 RGO:06603 cholesterol granuloma RGO:06603 RGO:06606 carcinoma of external auditory meatus RGO:06606 glial neoplasm HP:0009733 RADLEX:RID4026 SNOMEDCT:115240006 SNOMEDCT:393564001 SNOMEDCT:74532006 RGO:06607 glioma RGO:06607 RGO:06609 meningioma of Meckel cave RGO:06609 RGO:06613 erosion or widening of the internal auditory meatus RGO:06613 RGO:06617 glioma of brain stem RGO:06617 RGO:06622 dense temporal bone lesion RGO:06622 RGO:06627 temporal bone neoplasm RGO:06627 swimmer ear RADLEX:RID3664 RGO:06630 exostosis of external auditory canal RGO:06630 occipitalization of C1 RGO:06639 fusion of C1 to base of skull RGO:06639 DOID:2256 SNOMEDCT:67988000 RGO:06640 chondrodystrophy RGO:06640 HP:0002700 RGO:06641 enlarged foramen magnum RGO:06641 RGO:06645 surgical decompression RGO:06645 SNOMEDCT:26594006 RGO:06647 syringobulbia RGO:06647 emissary vein canal RGO:06669 inioindineal canal RGO:06669 ORDO:2500 SNOMEDCT:238872007 RGO:06683 acrogeria RGO:06683 RGO:06692 defective cranial ossification RGO:06692 HP:0004423 RGO:06697 cranium bifidum occultum RGO:06697 median cleft face syndrome median facial cleft syndrome ORDO:250 SNOMEDCT:254004006 RGO:06698 frontonasal dysplasia RGO:06698 RGO:06699 hypertelorism with Sprengel deformity RGO:06699 HP:0000237 RGO:06707 small anterior fontanelle RGO:06707 HP:0000270 RGO:06711 delayed closure of fontanelles RGO:06711 RGO:06712 cranium bifidum with lacunar skull RGO:06712 RGO:06715 severe rickets RGO:06715 SNOMEDCT:254253000 RGO:06718 fetal primidone syndrome RGO:06718 ORDO:2746 SNOMEDCT:254068007 RGO:06720 opsismodysplasia RGO:06720 RGO:06724 incomplete ossification of cranial sutures RGO:06724 DOID:2785 ICD10CM:Q03.1 SNOMEDCT:14447001 RGO:06725 Dandy-Walker syndrome RGO:06725 HP:0002084 SNOMEDCT:48777005 RGO:06730 cranium bifidum RGO:06730 Russell syndrome ORDO:1672 SNOMEDCT:237733001 RGO:06731 diencephalic syndrome RGO:06731 RGO:06735 prolonged parenteral hyperalimentation RGO:06735 idiopathic intracranial hypertension DOID:11459 RADLEX:RID4955 SNOMEDCT:68267002 RGO:06736 pseudotumor cerebri RGO:06736 RGO:06738 separation of cranial sutures in a child RGO:06738 RGO:06743 incomplete ossification adjacent to sutures RGO:06743 RGO:06750 hypervitaminosis A encephalopathy RGO:06750 RGO:06753 decreased cranial convolutional markings RGO:06753 RGO:06755 normal to age 3 years RGO:06755 RGO:06756 shunted hydrocephalus RGO:06756 RGO:06758 increased cranial convolutional markings RGO:06758 RGO:06762 secondary craniosynostosis RGO:06762 RGO:06763 large vascular grooves of skull RGO:06763 RGO:06764 hemangioma of skull RGO:06764 RGO:06766 metastasis to skull RGO:06766 RGO:06767 pacchionian granulations RGO:06767 RGO:06771 cyanotic congenital heart disease with secondary polycythemia RGO:06771 RGO:06772 hypernephroma with increased erythropoiesis RGO:06772 sunburst pattern sunburst skull RGO:06775 localized sunburst pattern in skull RGO:06775 DOID:3369 HP:0012254 ORDO:319 RADLEX:RID4522 SNOMEDCT:76909002 RGO:06777 Ewing sarcoma RGO:06777 RGO:06778 solitary intracranial calcification RGO:06778 RADLEX:RID13848 SNOMEDCT:264450003 SNOMEDCT:80621003 RGO:06781 choroid plexus RGO:06781 HP:0002888 ORDO:251636 RADLEX:RID4050 SNOMEDCT:443643007 SNOMEDCT:57706008 RGO:06795 ependymoma RGO:06795 HP:0006931 RGO:06802 lipoma of corpus callosum RGO:06802 RGO:06807 pituitary stone RGO:06807 RGO:06808 radiation necrosis RGO:06808 SNOMEDCT:64102008 RGO:06811 syphilitic gumma RGO:06811 HP:0002514 RGO:06812 multiple intracranial calcification RGO:06812 RGO:06820 carbon monoxide intoxication RGO:06820 DOID:8453 ICD10CM:E53.8 SNOMEDCT:190633005 RGO:06822 folic acid deficiency RGO:06822 DOID:11573 ICD10CM:A32 ORDO:533 SNOMEDCT:4241002 RGO:06832 listeriosis RGO:06832 RGO:06843 parasellar calcification RGO:06843 DOID:0110941 SNOMEDCT:254122007 RGO:06858 carbonic anhydrase II deficiency RGO:06858 Hallervorden-Spatz syndrome PKAN ORDO:157850 ORDO:216866 RGO:06861 pantothenate kinase-associated neurodegeneration RGO:06861 SNOMEDCT:51399001 RGO:06863 lead encephalopathy RGO:06863 mPKU mild PKU mild phenylketonuria variant PKU variant phenylketonuria ORDO:79253 RGO:06866 phenylketonuria variant RGO:06866 DOID:4183 ORDO:79445 SNOMEDCT:237659007 RGO:06867 pseudopseudohypoparathyroidism RGO:06867 ring-like intracranial calcification RGO:06869 curvilinear intracranial calcification RGO:06869 RADLEX:RID49914 RGO:06870 vascular abnormality RGO:06870 SNOMEDCT:38713004 RGO:06873 cystic astrocytoma RGO:06873 RGO:06874 cystic craniopharyngioma RGO:06874 DOID:1319 RGO:06882 primary brain tumor RGO:06882 DOID:3069 HP:0009592 ORDO:94 RADLEX:RID4027 SNOMEDCT:38713004 RGO:06883 astrocytoma RGO:06883 DOID:5241 HP:0010797 ORDO:252054 RADLEX:RID3995 SNOMEDCT:81201000 RGO:06889 hemangioblastoma RGO:06889 RADLEX:RID3899 SNOMEDCT:9287005 RGO:06892 colloid cyst RGO:06892 DOID:3304 HP:0100620 RADLEX:RID4315 SNOMEDCT:28307001 RGO:06902 germinoma RGO:06902 DOID:1664 HP:0030408 ORDO:251909 RADLEX:RID4491 SNOMEDCT:31671006 RGO:06903 pineoblastoma RGO:06903 HP:0030407 ORDO:251912 RADLEX:RID4493 SNOMEDCT:89096009 RGO:06904 pineocytoma RGO:06904 RGO:06913 supratentorial intracranial tumor in a child RGO:06913 RADLEX:RID4502 SNOMEDCT:128787000 RGO:06915 desmoplastic infantile ganglioglioma RGO:06915 DOID:3181 ORDO:251627 RADLEX:RID4078 SNOMEDCT:443936004 SNOMEDCT:73348003 RGO:06920 oligodendroglioma RGO:06920 DOID:3672 ORDO:69077 RADLEX:RID4424 SNOMEDCT:83118000 RGO:06922 rhabdoid tumor RGO:06922 RGO:06925 hypothalamic glioma RGO:06925 DOID:5648 HP:0030392 ORDO:251899 RADLEX:RID4084 SNOMEDCT:88252006 RGO:06938 choroid plexus carcinoma RGO:06938 RGO:06940 infratentorial intracranial tumor in a child RGO:06940 DOID:4202 RGO:06942 brain stem glioma RGO:06942 DOID:4848 RGO:06943 cerebellar astrocytoma RGO:06943 RGO:06948 skull base tumors RGO:06948 RGO:06949 brain tumor in an infant RGO:06949 RGO:06952 hypothalamic astrocytoma RGO:06952 metastasis to the brain RGO:06955 brain metastasis RGO:06955 RGO:06964 neoplastic solitary intracranial mass RGO:06964 RADLEX:RID5658 SNOMEDCT:255399007 RGO:06966 congenital RGO:06966 RGO:06967 cranial nerve origin RGO:06967 SNOMEDCT:127026004 RGO:06969 pineal tumor RGO:06969 RADLEX:RID11163 RGO:06970 intraventricular RGO:06970 RGO:06974 nonneoplastic solitary intracranial mass RGO:06974 RGO:06975 vascular lesion RGO:06975 HP:0001048 RADLEX:RID3973 SNOMEDCT:416824008 RGO:06977 cavernous angioma RGO:06977 RGO:06983 tumefactive multiple sclerosis RGO:06983 RADLEX:RID6403 RGO:06985 leptomeningeal RGO:06985 RGO:06987 multifocal intracranial lesions RGO:06987 RGO:07000 multiple nerve tumors RGO:07000 Louis-Bar syndrome ataxia-telangiectasia syndrome ORDO:100 RGO:07009 ataxia-telangiectasia RGO:07009 RGO:07013 hyperdense intracranial lesion RGO:07013 GBM DOID:3068 HP:0012174 RADLEX:RID4044 SNOMEDCT:393563007 SNOMEDCT:63634009 RGO:07020 glioblastoma multiforme RGO:07020 RGO:07025 isodense intracranial lesion RGO:07025 DOID:3829 HP:0002893 RADLEX:RID4220 SNOMEDCT:128664001 SNOMEDCT:254956000 RGO:07029 pituitary adenoma RGO:07029 RGO:07035 hypodense supratentorial lesion RGO:07035 HP:0002181 ICD10CM:G93.6 SNOMEDCT:2032001 RGO:07038 cerebral edema RGO:07038 HP:0012302 ORDO:1930 RGO:07047 herpes simplex encephalitis RGO:07047 DOID:5394 HP:0040278 ORDO:2965 SNOMEDCT:134209002 SNOMEDCT:34337008 RGO:07050 prolactinoma RGO:07050 intracranial lesion with homogeneous enhancement RGO:07052 homogeneously enhancing intracranial lesion RGO:07052 RGO:07056 markedly enhancing intracranial lesion RGO:07056 intracranial lesion with moderate enhancement RGO:07062 moderately enhancing intracranial lesion RGO:07062 DOID:2431 RADLEX:RID4512 SNOMEDCT:10438002 SNOMEDCT:403969002 RGO:07071 glomus tumor RGO:07071 intracranial lesion with minimal enhancement RGO:07078 minimally enhancing intracranial lesion RGO:07078 RGO:07090 multiple intracranial enhancing lesions RGO:07090 RGO:07102 ring-enhancing intracranial lesion RGO:07102 DOID:10080 ICD10CM:B70.1 SNOMEDCT:31659000 RGO:07114 sparganosis RGO:07114 DOID:4425 ICD10CM:D76.3 SNOMEDCT:189099001 SNOMEDCT:36279001 RGO:07123 xanthogranuloma RGO:07123 RGO:07127 pantopaque RGO:07127 RGO:07143 cystic encephalomalacia RGO:07143 HP:0001305 ORDO:217 SNOMEDCT:14447001 RGO:07147 Dandy-Walker malformation RGO:07147 RGO:07150 trapped fourth ventricle RGO:07150 DOID:0050902 HP:0002885 ORDO:616 RADLEX:RID4408 SNOMEDCT:443333004 SNOMEDCT:83217000 RGO:07158 medulloblastoma RGO:07158 ORDO:251639 RADLEX:RID4055 SNOMEDCT:4553004 RGO:07160 subependymoma RGO:07160 RGO:07168 gyriform cortical/subcortical T2 hypointensity RGO:07168 RGO:07175 gyriform cortical/subcortical T1 hyperintensity RGO:07175 RGO:07181 T2-hyperintense gyriform cortical lesion RGO:07181 RGO:07182 deep white matter and peripheral cortical infarction RGO:07182 RGO:07183 cryptococcoma with cryptococcal meningitis RGO:07183 RGO:07185 parenchymal metastases with cerebral carcinomatosis RGO:07185 SNOMEDCT:430051000124107 RGO:07187 viral meningoencephalitis RGO:07187 RGO:07197 intracranial lesion with hypointense ring RGO:07197 RADLEX:RID4338 RGO:07209 hamartoma of tuber cinereum RGO:07209 DOID:3642 ORDO:91354 SNOMEDCT:237722004 RGO:07228 empty sella syndrome RGO:07228 RGO:07232 pituitary abscess RGO:07232 RGO:07245 hypothalamic lesion RGO:07245 RGO:07246 ectopic posterior pituitary gland RGO:07246 RGO:07249 jugular foramen lesion RGO:07249 NHL DOID:0060060 HP:0012539 RADLEX:RID3843 SNOMEDCT:118601006 RGO:07255 non-Hodgkin lymphoma RGO:07255 RGO:07256 trigeminal nerve lesion RGO:07256 RGO:07263 middle cranial fossa lesion RGO:07263 RGO:07278 posterior skull base lesion RGO:07278 RGO:07286 radiation osteonecrosis RGO:07286 RGO:07294 rhabdomyosarcoma of nasopharynx RGO:07294 RGO:07296 extra-axial lesion RGO:07296 RGO:07313 idiopathic hypertrophic pachymeningitis RGO:07313 DOID:9471 HP:0001287 RADLEX:RID3494 SNOMEDCT:7180009 RGO:07314 meningitis RGO:07314 RGO:07320 midline supratentorial lesion RGO:07320 SNOMEDCT:21350002 RGO:07329 colloid cyst of third ventricle RGO:07329 HP:0012683 RGO:07332 pineal cyst RGO:07332 RGO:07334 cystic brain tumor with mural nodule RGO:07334 DOID:5078 ORDO:251949 RADLEX:RID4511 SNOMEDCT:87191000119100 SNOMEDCT:89880005 RGO:07335 ganglioglioma RGO:07335 DOID:4851 ORDO:251612 RADLEX:RID4029 SNOMEDCT:128854008 RGO:07338 pilocytic astrocytoma RGO:07338 DOID:4852 ORDO:251607 RADLEX:RID4031 SNOMEDCT:78838008 RGO:07339 pleomorphic xanthoastrocytoma RGO:07339 RGO:07340 intraventricular lesion RGO:07340 RADLEX:RID3910 SNOMEDCT:230792007 RGO:07344 ependymal cyst RGO:07344 RGO:07353 ventricular wall nodule RGO:07353 RGO:07354 heterotopic gray matter RGO:07354 DOID:10079 RGO:07355 neurocysticercosis RGO:07355 RGO:07361 thickened septum pellucidum RGO:07361 RGO:07363 noncommunicating cavum septi pellucidi RGO:07363 RGO:07367 posterior lateral ventricle lesion RGO:07367 HP:0002190 RADLEX:RID3898 SNOMEDCT:230790004 RGO:07369 choroid plexus cyst RGO:07369 DOID:10079 ICD10CM:B69 ORDO:1560 RADLEX:RID34758 SNOMEDCT:59051007 RGO:07370 cysticercosis RGO:07370 RGO:07373 lateral ventricle body lesion RGO:07373 RGO:07374 anterior third ventricle lesion RGO:07374 DOID:5077 ORDO:251618 RADLEX:RID4033 SNOMEDCT:1586004 SNOMEDCT:449799008 RGO:07376 subependymal giant cell astrocytoma RGO:07376 RGO:07378 posterior third ventricle lesion RGO:07378 RGO:07381 cystic pineal gland RGO:07381 RGO:07383 quadrigeminal cyst RGO:07383 RGO:07385 pineal region lesion RGO:07385 RGO:07391 fourth ventricular lesion RGO:07391 RGO:07393 cerebellar lesion RGO:07393 infarct infarcts RADLEX:RID5172 SNOMEDCT:55641003 RGO:07395 infarction RGO:07395 RGO:07396 hypoplasia or aplasia of cerebellum RGO:07396 RGO:07402 posterior fossa lesion RGO:07402 RGO:07408 cerebellopontine angle lesion RGO:07408 RGO:07415 posterior fossa tumor in a child RGO:07415 RGO:07421 posterior fossa cystic lesion RGO:07421 RGO:07425 giant cisterna magna RGO:07425 RGO:07436 fourth ventricle outlet obstruction RGO:07436 SNOMEDCT:414400006 RGO:07442 tonsillar herniation RGO:07442 HP:0012755 RGO:07444 enlarged brainstem RGO:07444 metastatic disease RADLEX:RID49953 RADLEX:RID5231 RGO:07445 metastasis RGO:07445 DOID:9588 HP:0002383 RADLEX:RID3411 SNOMEDCT:45170000 RGO:07446 encephalitis RGO:07446 RADLEX:RID39485 RGO:07451 vascular anomaly RGO:07451 osmotic demyelination DOID:636 ICD10CM:G37.2 RADLEX:RID5050 SNOMEDCT:6807001 RGO:07455 central pontine myelinolysis RGO:07455 DOID:11389 SNOMEDCT:37660004 RGO:07457 subdural empyema RGO:07457 RGO:07464 linear meningeal enhancement RGO:07464 RGO:07467 diffuse gyriform meningeal enhancement RGO:07467 RGO:07474 rheumatoid pachymeningitis RGO:07474 RGO:07477 localized gyriform meningeal enhancement RGO:07477 RGO:07480 ependymal enhancement RGO:07480 RGO:07486 hyperdense basilar cisterns RGO:07486 HP:0002138 RADLEX:RID4710 SNOMEDCT:21454007 RGO:07488 subarachnoid hemorrhage RGO:07488 SNOMEDCT:410071005 RGO:07490 bromism RGO:07490 RGO:07494 basilar cistern intense enhancement RGO:07494 DOID:10328 ICD10CM:J63.4 SNOMEDCT:62371005 RGO:07499 siderosis RGO:07499 RGO:07500 intracranial fat RGO:07500 RADLEX:RID4800 SNOMEDCT:14415006 RGO:07502 pneumocephalus RGO:07502 RGO:07508 congenital brain malformation RGO:07508 RGO:07510 enceophalocele RGO:07510 HP:0002282 RADLEX:RID3742 SNOMEDCT:128490007 RGO:07512 heterotopia RGO:07512 agyria DOID:0050453 HP:0001339 ICD10CM:Q04.3 RADLEX:RID3766 SNOMEDCT:204036008 RGO:07513 lissencephaly RGO:07513 HP:0001302 ICD10CM:Q04.3 RADLEX:RID3764 SNOMEDCT:23024003 RGO:07514 pachygyria RGO:07514 HP:0002126 ORDO:35981 RADLEX:RID3768 SNOMEDCT:4945003 RGO:07515 polymicrogyria RGO:07515 HP:0010636 ICD10CM:Q04.6 ORDO:799 SNOMEDCT:253159001 RGO:07516 schizencephaly RGO:07516 corpus callosum agenesis HP:0001274 RGO:07518 agenesis of the corpus callosum RGO:07518 HPE arrhinencephaly DOID:4621 HP:0001360 ICD10CM:Q04.2 ORDO:2162 SNOMEDCT:30915001 RGO:07521 holoprosencephaly RGO:07521 absent or hypoplastic septum pellucidum DOID:0060857 HP:0100842 ORDO:3157 RGO:07522 septo-optic dysplasia RGO:07522 RGO:07524 encephalitis and meningitis RGO:07524 DOID:3431 RADLEX:RID3411 RGO:07527 cerebritis RGO:07527 DOID:10699 ICD10CM:B66.4 SNOMEDCT:30369007 RGO:07533 paragonimiasis RGO:07533 RGO:07536 Epstein-Barr encephalitis RGO:07536 RGO:07539 bacterial meningitis RGO:07539 RGO:07540 viral meningitis RGO:07540 RGO:07541 postmeningitis RGO:07541 RGO:07546 degenerative and metabolic disorders RGO:07546 DOID:10652 HP:0002511 RADLEX:RID5137 SNOMEDCT:26929004 RGO:07547 Alzheimer disease RGO:07547 DOID:14784 HP:0002542 SNOMEDCT:67761004 RGO:07551 olivopontocerebellar atrophy RGO:07551 DOID:11870 RADLEX:RID5140 SNOMEDCT:13092008 RGO:07552 pick disease RGO:07552 Steele-Richardson-Olszewski syndrome ORDO:240071 RGO:07553 progressive supranuclear palsy RGO:07553 DOID:4752 ORDO:98932 SNOMEDCT:16576004 RGO:07554 Shy-Drager syndrome RGO:07554 DOID:4751 ICD10CM:G23.2 SNOMEDCT:29618004 RGO:07555 striatonigral degeneration RGO:07555 SNEM subacute necrotizing encephalomyelopathy DOID:3652 ORDO:506 SNOMEDCT:29570005 RGO:07557 Leigh disease RGO:07557 RGO:07559 nonketotic hyperglycemia RGO:07559 RGO:07561 dysmyelinating disease RGO:07561 DOID:9269 ORDO:511 SNOMEDCT:27718001 RGO:07571 maple syrup urine disease RGO:07571 DOID:4252 ORDO:58 SNOMEDCT:81854007 RGO:07573 Alexander disease RGO:07573 DOID:3213 RADLEX:RID5048 RGO:07575 demyelinating disease RGO:07575 DOID:10992 RGO:07578 acute hemorrhagic encephalomyelitis RGO:07578 RGO:07579 carbon monxide encephalopathy RGO:07579 spongiform encephalopathy DOID:11949 SNOMEDCT:792004 RGO:07583 Jakob-Creutzfeldt disease RGO:07583 myelinoclastic diffuse sclerosis DOID:10588 ORDO:59298 SNOMEDCT:49692006 RGO:07587 Schilder disease RGO:07587 DOID:8970 ICD10CM:A81.1 SNOMEDCT:192685000 RGO:07588 subacute sclerosing panencephalitis RGO:07588 SNOMEDCT:29658002 RGO:07593 anoxia RGO:07593 HP:0030049 SNOMEDCT:441806004 RGO:07594 brain abscess RGO:07594 RGO:07596 deficiency syndromes RGO:07596 RGO:07598 periventricular T2 hyperintense lesion RGO:07598 SNOMEDCT:230698000 RGO:07606 lacunar infarction RGO:07606 RGO:07614 transependymal CSF flow RGO:07614 RGO:07615 periventricular hypodense lesion RGO:07615 RGO:07616 cystic neoplasm RGO:07616 DOID:2034 HP:0040197 RADLEX:RID39076 SNOMEDCT:58762006 RGO:07617 encephalomalacia RGO:07617 DOID:3526 ICD10CM:I63 SNOMEDCT:432504007 RGO:07619 cerebral infarction RGO:07619 RGO:07624 left atrial myxoma RGO:07624 RGO:07625 nonvalvular atrial fibrillation RGO:07625 DOID:4079 HP:0001654 RADLEX:RID3260 SNOMEDCT:368009 RGO:07626 valvular heart disease RGO:07626 RADLEX:RID3312 RGO:07630 amyloid angiopathy RGO:07630 RADLEX:RID3326 SNOMEDCT:22039006 RGO:07635 ruptured aneurysm RGO:07635 SNOMEDCT:419076005 RGO:07639 allergic reaction RGO:07639 RGO:07642 near-drowning RGO:07642 RGO:07643 primary central respiratory failure RGO:07643 RGO:07644 heredity RGO:07644 SNOMEDCT:365981007 RGO:07648 smoking RGO:07648 HP:0001342 RGO:07650 intracerebral hemorrhage RGO:07650 RGO:07664 hypertensive intracerebral hemorrhage RGO:07664 RGO:07669 lack of filling of intracranial vessels RGO:07669 RADLEX:RID3317 SNOMEDCT:122459003 SNOMEDCT:5399005 RGO:07672 dissection RGO:07672 RADLEX:RID4969 SNOMEDCT:125319009 SNOMEDCT:257351008 RGO:07674 shunt RGO:07674 RGO:07676 intracranial hypervascularity RGO:07676 RGO:07678 congenital variant RGO:07678 RGO:07680 increased intracranial vessel size RGO:07680 RADLEX:RID4854 RGO:07681 carotid-cavernous fistula RGO:07681 RADLEX:RID4743 SNOMEDCT:25322007 RGO:07682 ectasia RGO:07682 RGO:07683 high flow system RGO:07683 RGO:07684 decreased intracranial vessel size RGO:07684 RGO:07685 low flow system RGO:07685 RGO:07688 cerebral vessel wall irregularity RGO:07688 SNOMEDCT:112670000 RGO:07689 fibromuscular hyperplasia RGO:07689 RADLEX:RID4814 SNOMEDCT:45352006 RGO:07690 spasm RGO:07690 RGO:07692 prolonged cerebral vascular transit time RGO:07692 RGO:07693 focal edema RGO:07693 RGO:07696 decreased cerebral vascular transit time RGO:07696 RGO:07697 increased pCO RGO:07697 RGO:07705 radiation arteritis RGO:07705 RGO:07706 rickettsial arteritis RGO:07706 RGO:07707 sarcoid arteritis RGO:07707 RGO:07708 syphilitic arteritis RGO:07708 RGO:07709 tuberculous arteritis RGO:07709 DOID:3527 RGO:07711 cerebral arterial disease RGO:07711 RGO:07722 intracranial arteriovenous shunting RGO:07722 HP:0004950 RGO:07724 occlusive vascular disease RGO:07724 DOID:11390 SNOMEDCT:28366008 RGO:07726 cerebral arteritis RGO:07726 RGO:07730 intracerebral hematoma RGO:07730 RGO:07731 avascular intracranial mass RGO:07731 RADLEX:RID4702 SNOMEDCT:125667009 SNOMEDCT:308492005 RGO:07732 contusion RGO:07732 HP:0000969 RADLEX:RID4865 SNOMEDCT:267038008 SNOMEDCT:423666004 SNOMEDCT:79654002 RGO:07733 edema RGO:07733 RGO:07741 avascular zone near the brain surface RGO:07741 HP:0002120 RGO:07742 cortical atrophy RGO:07742 RGO:07747 syphilitic pachymeningitis RGO:07747 RGO:07748 brain ischemia secondary to extracranial lesion RGO:07748 DOID:13002 SNOMEDCT:15258001 RGO:07755 subclavian steal syndrome RGO:07755 HP:0010775 SNOMEDCT:110409004 SNOMEDCT:66403007 RGO:07761 vascular ring RGO:07761 RGO:07762 intracranial lesion in an infant RGO:07762 HP:0001331 RGO:07764 absent septum pellucidum RGO:07764 RGO:07770 mineralizing vasculopathy RGO:07770 RGO:07773 echogenic brain lesion RGO:07773 SNOMEDCT:15158005 SNOMEDCT:417696007 RGO:07776 intracranial air RGO:07776 PVL DOID:13088 HP:0006970 ICD10CM:P91.2 ORDO:171676 SNOMEDCT:230769007 RGO:07777 periventricular leukomalacia RGO:07777 HP:0002664 RADLEX:RID3957 SNOMEDCT:108369006 RGO:07778 tumor RGO:07778 RGO:07779 cystic brain lesion RGO:07779 RGO:07780 leptomenigeal cyst RGO:07780 HP:0001305 RGO:07783 Dandy-Walker cyst RGO:07783 RGO:07786 ventricular cyst RGO:07786 RGO:07787 high-resistance internal carotid artery flow RGO:07787 RGO:07789 distal internal carotid artery stenosis RGO:07789 RGO:07790 distal small vessel disease RGO:07790 RGO:07791 low cardiac output RGO:07791 RGO:07792 low-velocity internal carotid artery flow RGO:07792 DOID:1712 HP:0001650 SNOMEDCT:60573004 RGO:07793 aortic valve stenosis RGO:07793 RGO:07794 proximal internal carotid artery stenosis RGO:07794 RGO:07795 tandem lesions RGO:07795 DOID:10824 SNOMEDCT:70272006 RGO:07799 malignant hypertension RGO:07799 HP:0002410 RGO:07803 aqueductal stenosis RGO:07803 DOID:9972 ICD10CM:E67.0 SNOMEDCT:64559002 RGO:07807 hypervitaminosis A RGO:07807 SNOMEDCT:69791001 RGO:07808 increased venous pressure RGO:07808 HP:0002516 RADLEX:RID34800 SNOMEDCT:271719001 RGO:07810 increased intracranial pressure RGO:07810 RGO:07811 increased craniofacial ratio RGO:07811 RGO:07812 increased digital markings of calvarium RGO:07812 RGO:07815 thinning of calvarium RGO:07815 fetal ventriculomegaly hydrocephaly DOID:10908 HP:0000238 ICD10CM:G91 RADLEX:RID4885 SNOMEDCT:230745008 RGO:07816 hydrocephalus RGO:07816 RGO:07822 hypertensive cerebral degenerative disease RGO:07822 RADLEX:RID5148 SNOMEDCT:56267009 RGO:07823 multi-infarct dementia RGO:07823 RGO:07824 normal aging RGO:07824 RGO:07840 developmental stenosis RGO:07840 RGO:07845 brain-stem edema RGO:07845 CPA tumor DOID:3200 SNOMEDCT:126947009 RGO:07846 cerebellopontine angle tumor RGO:07846 ICD10CM:Q03 ORDO:2185 SNOMEDCT:47032000 RGO:07853 congenital hydrocephalus RGO:07853 DOID:8461 ORDO:50 SNOMEDCT:80651009 RGO:07855 Aicardi syndrome RGO:07855 RGO:07858 bobble-head doll syndrome RGO:07858 SNOMEDCT:18311000119109 RGO:07864 infant of diabetic mother RGO:07864 ORDO:2330 SNOMEDCT:86635005 RGO:07865 Kasabach-Merritt syndrome RGO:07865 DOID:10581 ICD10CM:E75.25 ORDO:512 RADLEX:RID34778 SNOMEDCT:396338004 RGO:07868 metachromatic leukodystrophy RGO:07868 pseudothalidomide syndrome DOID:5325 ORDO:3103 RGO:07872 Roberts syndrome RGO:07872 fetal triploidy syndrome ORDO:3376 RGO:07873 triploidy RGO:07873 RGO:07879 large head in infant RGO:07879 RGO:07882 intracranial cyst RGO:07882 HP:0002684 RGO:07886 calvarial thickening RGO:07886 RGO:07888 large ventricle in infant RGO:07888 SNOMEDCT:254935002 RGO:07891 intracranial tumor RGO:07891 RGO:07896 small cerebral ventricles RGO:07896 RGO:07899 abnormal configuration of cerebral ventricles RGO:07899 Huntington chorea DOID:12858 ORDO:399 RADLEX:RID5154 RGO:07903 Huntington disease RGO:07903 HP:0100571 RGO:07905 ventricular diverticulum RGO:07905 CSF rhinorrhea SNOMEDCT:85638002 RGO:07906 cerebrospinal fluid rhinorrhea RGO:07906 human immunodeficiency virus infection DOID:526 SNOMEDCT:86406008 RGO:07912 HIV infection RGO:07912 RGO:07916 protozoal infection RGO:07916 DOID:12157 ICD10CM:G03.0 SNOMEDCT:301770000 RGO:07924 aseptic meningitis RGO:07924 SNOMEDCT:230202002 RGO:07925 vacuolar myelopathy RGO:07925 RGO:07927 acute polyradiculoneuropathy RGO:07927 ORDO:2932 SNOMEDCT:444728005 RGO:07928 chronic inflammatory demyelinating polyneuropathy RGO:07928 RGO:07929 distal symmetrical axonal polyneuropathy RGO:07929 DOID:1835 ICD10CM:G58.7 SNOMEDCT:30292005 RGO:07930 mononeuritis multiplex RGO:07930 RGO:07931 malformed orbit RGO:07931 SNOMEDCT:112481007 SNOMEDCT:205798005 RGO:07937 cyclops RGO:07937 RGO:07944 acrofrontonasal dysostosis RGO:07944 CHARGE association DOID:0050834 ORDO:138 RGO:07945 CHARGE syndrome RGO:07945 RGO:07946 chromosome 20:dup(20p) syndrome RGO:07946 RGO:07948 intrauterine growth retardation syndrome RGO:07948 RGO:07949 postaxial acrofacial dysostosis Miller type RGO:07949 craniosynostosis with premature closure of metopic suture HP:0000243 ICD10CM:Q75.0 SNOMEDCT:28740008 RGO:07950 trigonocephaly RGO:07950 RGO:07954 craniosynostosis of coronal sutures RGO:07954 HP:0012720 RGO:07958 nasal tumor RGO:07958 ocular hypertelorism orbital hypertelorism HP:0000316 ICD10CM:Q75.2 SNOMEDCT:22006008 RGO:07959 hypertelorism RGO:07959 Franceschetti-Klein syndrome Treacher Collins-Franceschetti syndrome mandibulofacial dysostosis mandibulofacial dysostosis without limb anomalies DOID:2908 HP:0005321 ICD10CM:Q75.4 ORDO:861 SNOMEDCT:82203000 RGO:07963 Treacher Collins syndrome RGO:07963 ORDO:124 SNOMEDCT:88854002 RGO:07968 Diamond-Blackfan syndrome RGO:07968 Pena-Shokeir syndrome type 1 ORDO:994 RGO:07971 fetal akinesia deformation sequence RGO:07971 SNOMEDCT:9527009 RGO:07977 Pallister-Killian syndrome RGO:07977 RGO:07982 enucleation in childhood RGO:07982 HP:0000648 SNOMEDCT:76976005 RGO:07983 optic nerve atrophy RGO:07983 HP:0004440 RGO:07993 coronal craniosynostosis RGO:07993 RGO:07999 hypoplastic maxilla RGO:07999 RGO:08002 varix of orbital vein RGO:08002 RGO:08003 orbital mass RGO:08003 SNOMEDCT:82576008 RGO:08005 intraocular foreign body RGO:08005 RGO:08006 meningioma of optic nerve RGO:08006 HP:0009734 SNOMEDCT:404662003 RGO:08007 optic glioma RGO:08007 RGO:08008 benign infantile myxofibromatosis RGO:08008 RGO:08009 choroidal osteoma RGO:08009 RGO:08012 ophthalmic artery aneurysm RGO:08012 DOID:1210 HP:0100653 ICD10CM:H46 RADLEX:RID28824 SNOMEDCT:66760008 RGO:08013 optic neuritis RGO:08013 DOID:768 HP:0009919 ORDO:790 RADLEX:RID4472 SNOMEDCT:19906005 SNOMEDCT:370967009 RGO:08014 retinoblastoma RGO:08014 RGO:08018 intraocular mass in a child RGO:08018 RGO:08024 chronic retinal detachment RGO:08024 RGO:08025 coat disease RGO:08025 DOID:13141 HP:0000554 SNOMEDCT:128473001 RGO:08029 uveitis RGO:08029 RGO:08030 choroidal mass RGO:08030 SNOMEDCT:94254004 RGO:08031 metastasis to choroid RGO:08031 DOID:2681 HP:0003764 SNOMEDCT:21119008 RGO:08034 nevus RGO:08034 SNOMEDCT:52357004 RGO:08035 retinal cyst RGO:08035 RGO:08036 retinal gliosis RGO:08036 RGO:08037 extraconal orbital lesion RGO:08037 RGO:08039 lacrimal gland tumor RGO:08039 DOID:9938 HP:0000620 SNOMEDCT:85777005 RGO:08042 dacryocystitis RGO:08042 DOID:9369 ICD10CM:H05.12 SNOMEDCT:80698001 RGO:08044 orbital myositis RGO:08044 RGO:08045 extraorbital extracranial lesion extending to the orbit RGO:08045 olfactory neuroblastoma ORDO:1957 RADLEX:RID4432 SNOMEDCT:422886007 SNOMEDCT:76060004 RGO:08053 esthesioneuroblastoma RGO:08053 RGO:08058 intracranial lesion involving the orbit RGO:08058 RGO:08060 chiasmatic arachnoiditis RGO:08060 SNOMEDCT:52330001 RGO:08061 encephalomeningocele RGO:08061 RGO:08062 hypothalamic tumor RGO:08062 orbital erosion radiolucent lesion of the orbit RGO:08067 orbital bony defect RGO:08067 SNOMEDCT:302857002 SNOMEDCT:60392001 RGO:08072 juvenile angiofibroma RGO:08072 RGO:08075 orbital wall sclerosis RGO:08075 DOID:293 RGO:08078 lacrimal gland carcinoma RGO:08078 narrowed sphenoidal fissure RGO:08081 narrowed superior orbital fissure RGO:08081 enlarged sphenoidal fissure RGO:08086 enlarged superior orbital fissure RGO:08086 RGO:08088 normal asymmetry RGO:08088 SNOMEDCT:231853000 RGO:08094 orbital varix RGO:08094 RGO:08095 posterior orbital encephalocele RGO:08095 localized erosion about the optic canal RGO:08097 localized bony defect about the optic canal RGO:08097 RGO:08103 surgical defect RGO:08103 RGO:08104 optic canal enlargement RGO:08104 DOID:5632 SNOMEDCT:254978007 RGO:08105 optic nerve sheath meningioma RGO:08105 RGO:08113 optic nerve enlargement RGO:08113 DOID:2450 ICD10CM:H34.81 SNOMEDCT:68478007 RGO:08118 central retinal vein occlusion RGO:08118 RGO:08120 cyst of optic nerve sheath RGO:08120 HP:0100775 RADLEX:RID34747 RGO:08121 dural ectasia RGO:08121 hematomas RADLEX:RID4705 SNOMEDCT:35566002 SNOMEDCT:385494008 RGO:08123 hematoma RGO:08123 RGO:08126 radiation-induced optic neuropathy RGO:08126 SNOMEDCT:48233004 RGO:08127 trauma to optic nerve RGO:08127 perineural enhancement of the optic nerve RGO:08129 optic nerve tram-track sign RGO:08129 Chester-Erdheim disease DOID:4329 ORDO:35687 RADLEX:RID3852 SNOMEDCT:699537002 SNOMEDCT:703711007 RGO:08131 Erdheim-Chester disease RGO:08131 RGO:08133 perioptic hemorrhage RGO:08133 RGO:08134 enlarged orbital rectus muscles RGO:08134 HP:0031622 SNOMEDCT:35929003 RGO:08136 Brown syndrome RGO:08136 IgG4-related dacryoadenitis and sialoadenitis Mikulicz disease chronic dacryoadenitis and sialoadenitis ORDO:79078 SNOMEDCT:7826003 RGO:08142 Mikulicz syndrome RGO:08142 painful oththalmoplegia superior orbital fissuritis DOID:1278 ORDO:64686 RADLEX:RID3673 SNOMEDCT:95794005 RGO:08147 Tolosa-Hunt syndrome RGO:08147 unilateral proptosis RGO:08150 unilateral exophthalmos RGO:08150 SNOMEDCT:232398002 RGO:08156 paranasal sinus osteoma RGO:08156 RGO:08168 orbital varices RGO:08168 RGO:08172 eyeball deformity RGO:08172 HP:0031730 SNOMEDCT:408757002 RGO:08173 axial myopia RGO:08173 RGO:08174 coloboma of globe RGO:08174 HP:0000667 ICD10CM:H44.52 RADLEX:RID5170 SNOMEDCT:4229009 RGO:08177 phthisis bulbi RGO:08177 RGO:08178 surgical scleral banding RGO:08178 HP:0007707 ICD10CM:H27.0 SNOMEDCT:24010005 RGO:08179 aphakia RGO:08179 ICD10CM:Q11.3 SNOMEDCT:93181004 RGO:08181 macrophthalmos RGO:08181 HP:0030856 SNOMEDCT:87819007 RGO:08182 posterior staphyloma RGO:08182 SNOMEDCT:419596007 RGO:08183 subchoroidal hemorrhage RGO:08183 DOID:12132 RADLEX:RID3702 SNOMEDCT:195353004 RGO:08184 Wegener granulomatosis RGO:08184 HP:0011510 SNOMEDCT:18695008 RGO:08192 drusen RGO:08192 DOID:1686 HP:0000501 ICD10CM:H40 SNOMEDCT:23986001 RGO:08193 glaucoma RGO:08193 RGO:08198 mucocele invading orbit RGO:08198 RGO:08201 phakoma RGO:08201 RGO:08203 globe calcification RGO:08203 RGO:08205 sarcoidosis of optic nerve sheath RGO:08205 RGO:08206 foreign body in globe RGO:08206 retrolental fibrodysplasia DOID:13025 ICD10CM:H35.17 RADLEX:RID3362 SNOMEDCT:415297005 RGO:08210 retrolental fibroplasia RGO:08210 RGO:08212 extraglobal calcification RGO:08212 RGO:08215 lacrimal gland neoplasm RGO:08215 RGO:08218 periorbital soft-tissue swelling RGO:08218 RGO:08220 orbital inflammation RGO:08220 RGO:08221 lacrimal gland enlargement RGO:08221 SNOMEDCT:19750001 RGO:08226 benign lymphoid hyperplasia RGO:08226 DOID:12185 HP:0000362 ICD10CM:H80 RADLEX:RID3527 SNOMEDCT:11543004 RGO:08253 otosclerosis RGO:08253 RGO:08255 facial canal lesion within temporal bone RGO:08255 RGO:08260 malignant external otitis RGO:08260 DOID:0050773 HP:0002668 RADLEX:RID4512 SNOMEDCT:302833002 SNOMEDCT:803009 RGO:08261 paraganglioma RGO:08261 RGO:08264 facial nerve lesion outside the temporal bone RGO:08264 ORDO:2810 RGO:08265 idiopathic facial nerve palsy RGO:08265 HP:0010628 RGO:08269 facial nerve palsy RGO:08269 DOID:12506 SNOMEDCT:193093009 RGO:08270 Bell palsy RGO:08270 DOID:9210 SNOMEDCT:21954000 RGO:08272 herpes zoster oticus RGO:08272 RGO:08274 temporal bone osteolysis RGO:08274 RGO:08280 destructive lesion in petrous apex RGO:08280 RGO:08282 abscess of petrous apex RGO:08282 Gradenigo-Lannois syndrome apical petrositis SNOMEDCT:37936001 RGO:08283 Gradenigo syndrome RGO:08283 RGO:08287 chondrosarcoma of skull base RGO:08287 RGO:08288 vascular middle ear mass RGO:08288 ICD10CM:I72.0 SNOMEDCT:233988005 RGO:08290 aneurysm of carotid artery RGO:08290 RGO:08292 exposed, high-riding jugular bulb RGO:08292 HP:0011475 RGO:08294 persistent stapedial artery RGO:08294 RGO:08295 soft tissue in the middle ear RGO:08295 HP:0000389 SNOMEDCT:21186006 RGO:08297 chronic otitis media RGO:08297 SNOMEDCT:253031000 RGO:08298 glomus tympanicum tumor RGO:08298 RADLEX:RID3819 SNOMEDCT:61363009 RGO:08299 granulation tissue RGO:08299 DOID:869 HP:0009797 RADLEX:RID3950 SNOMEDCT:363668000 SNOMEDCT:575006 RGO:08301 cholesteatoma RGO:08301 HP:0010628 SNOMEDCT:280816001 RGO:08302 facial nerve paralysis RGO:08302 ICD10CM:H83.1 SNOMEDCT:89097000 RGO:08303 labyrinthine fistula RGO:08303 RGO:08304 sinus thrombosis RGO:08304 RGO:08313 ceruminous gland tumor RGO:08313 RADLEX:RID3477 SNOMEDCT:59370009 SNOMEDCT:68220001 RGO:08317 keratosis obturans RGO:08317 HP:0012721 RADLEX:RID3337 SNOMEDCT:234124003 RGO:08322 venous malformation RGO:08322 DOID:0060322 HP:0000265 RADLEX:RID3489 SNOMEDCT:52404001 RGO:08323 mastoiditis RGO:08323 Buckley syndrome Job syndrome hyper-IgE syndrome hyperimmunoglobulin E syndrome RGO:08325 hyperimmunoglobulinemia E syndrome RGO:08325 DOID:9169 ICD10CM:D82.0 ORDO:906 SNOMEDCT:36070007 RGO:08327 Wiskott-Aldrich syndrome RGO:08327 RGO:08328 underdevelopment of mastoids RGO:08328 RGO:08331 increased pneumatization of mastoids RGO:08331 bony narrowing of external auditory canal HP:0000402 RGO:08332 external auditory canal stenosis RGO:08332 RGO:08334 congenital rubeola RGO:08334 ORDO:3312 RGO:08337 thalidomide embryopathy RGO:08337 postoperative change RGO:08341 postsurgical changes RGO:08341 RGO:08342 recurrent external otitis RGO:08342 RGO:08343 external auditory canal tumor RGO:08343 RGO:08350 retroauricular proliferating hemangioma RGO:08350 calcification in pinna calcified pinnae ossification of pinnae HP:0005103 RGO:08352 ear cartilage calcification RGO:08352 SNOMEDCT:370977006 SNOMEDCT:38045000 RGO:08354 frostbite RGO:08354 DOID:13189 HP:0001997 ICD10CM:M10 RADLEX:RID3567 SNOMEDCT:90560007 RGO:08355 gout RGO:08355 DOID:13774 HP:0008207 ORDO:85138 SNOMEDCT:363732003 RGO:08356 Addison disease RGO:08356 CPPD calcium pyrophosphate deposition disease calcium pyrophosphate dihydrate deposition disease tophaceous pseudogout RGO:08357 calcium pyrophosphate dihydrate crystal deposition disease RGO:08357 ORDO:47045 RGO:08358 familial cold hypersensitivity RGO:08358 ORDO:85202 RGO:08362 Keutel syndrome RGO:08362 ochronosis DOID:9270 ICD10CM:E70.29 ORDO:56 SNOMEDCT:360381004 RGO:08363 alkaptonuria RGO:08363 RGO:08366 syphilitic perichondritis RGO:08366 RGO:08368 nasal cavity lesion RGO:08368 RGO:08375 antrochoanal polyp RGO:08375 DOID:3355 HP:0100244 ORDO:2030 RADLEX:RID4300 SNOMEDCT:443250000 SNOMEDCT:53654007 RGO:08381 fibrosarcoma RGO:08381 DOID:3179 SNOMEDCT:104081000119103 SNOMEDCT:90121000 RGO:08383 inverted papilloma RGO:08383 RGO:08385 unilateral nasal cavity mass RGO:08385 SNOMEDCT:60392001 RGO:08388 nasopharyngeal angiofibroma RGO:08388 RGO:08390 nasal septum perforation RGO:08390 scleroma DOID:11336 RADLEX:RID3719 SNOMEDCT:72409005 RGO:08394 rhinoscleroma RGO:08394 RGO:08395 nasal ridge mass in a child RGO:08395 ORDO:141118 SNOMEDCT:65455002 RGO:08399 nasal encephalocele RGO:08399 RADLEX:RID3773 SNOMEDCT:5645008 RGO:08400 nasal glioma RGO:08400 DOID:9856 ICD10CM:A50 SNOMEDCT:35742006 RGO:08403 congenital syphilis RGO:08403 SNOMEDCT:19633006 RGO:08411 mucous retention cyst RGO:08411 HP:0009796 SNOMEDCT:59857007 RGO:08414 branchial cleft cyst RGO:08414 DOID:2602 RADLEX:RID4126 SNOMEDCT:31186001 RGO:08415 chondroma RGO:08415 ICD10CM:K09.0 RADLEX:RID3903 SNOMEDCT:9245008 RGO:08416 dentigerous cyst RGO:08416 SNOMEDCT:43917008 RGO:08420 giant cell granuloma RGO:08420 SNOMEDCT:419366003 SNOMEDCT:419893006 RGO:08421 inclusion cyst RGO:08421 ICD10CM:K09.1 SNOMEDCT:90516007 RGO:08422 nasoalveolar cyst RGO:08422 DOID:8485 ICD10CM:B46 ORDO:73263 SNOMEDCT:59277005 RGO:08427 zygomycosis RGO:08427 DOID:264 RADLEX:RID3997 SNOMEDCT:134335004 SNOMEDCT:36060005 RGO:08431 hemangiopericytoma RGO:08431 RGO:08436 cystic nasopharyngeal mass RGO:08436 RGO:08437 atypical lymph node RGO:08437 SNOMEDCT:60100005 RGO:08438 pharyngeal cyst RGO:08438 RADLEX:RID3941 RGO:08439 tornwaldt cyst RGO:08439 RGO:08440 destructive nasopharyngeal mass in a child RGO:08440 RGO:08443 minor salivary gland tumor RGO:08443 RGO:08445 nasopharyngeal extension of intracranial neoplasm RGO:08445 DOID:3828 SNOMEDCT:37039006 RGO:08446 chromophobe adenoma RGO:08446 sphenomaxillary fossa lesions RGO:08465 pterygopalatine fossa lesion RGO:08465 post-styloid parapharyngeal space mass RGO:08475 carotid space mass RGO:08475 RGO:08476 enlarged lateral retropharyngeal lymph node RGO:08476 RGO:08479 parapharyngeal space lesion RGO:08479 RGO:08481 epidermoid inclusion cyst RGO:08481 SNOMEDCT:19928005 RGO:08482 fibromatosis RGO:08482 RGO:08483 jugular vein thrombosis RGO:08483 mixed tumor DOID:452 RADLEX:RID4544 SNOMEDCT:8360001 RGO:08486 pleomorphic adenoma RGO:08486 RGO:08489 fatty parapharyngeal space lesion RGO:08489 DOID:3616 RADLEX:RID4344 SNOMEDCT:404057003 SNOMEDCT:73219006 RGO:08490 angiolipoma RGO:08490 Launois-Bensaude adenolipomatosis benign symmetric lipomatosis benign symmetric lipomatosis of Launois-Bensaude central non-encapsulated lipomatosis cephalothoracic lipodystrophy familial benign cervical lipomatosis multiple symmetric lipomatosis RADLEX:RID3866 RGO:08491 Madelung disease RGO:08491 RADLEX:RID4349 SNOMEDCT:404064001 SNOMEDCT:77027006 RGO:08493 hibernoma RGO:08493 RGO:08495 masticator space lesion RGO:08495 RADLEX:RID39000 SNOMEDCT:48607003 RGO:08497 accessory parotid gland RGO:08497 RGO:08498 benign masseteric hypertrophy RGO:08498 RGO:08503 congenital pharyngeal abnormality RGO:08503 DOID:9574 HP:0000453 ICD10CM:Q30.0 ORDO:137914 RADLEX:RID3736 SNOMEDCT:204508009 RGO:08504 choanal atresia RGO:08504 RGO:08507 functional pharyngeal disorder RGO:08507 RGO:08510 traumatic pharyngeal disorder RGO:08510 RGO:08514 pharyngeal infection RGO:08514 DOID:0060119 HP:0100638 RGO:08518 pharyngeal neoplasm RGO:08518 RGO:08528 paranasal sinus opacification RGO:08528 RGO:08537 polypoid rhinosinusitis RGO:08537 RGO:08538 fluid level in a paranasal sinus RGO:08538 RGO:08539 sinus wall fracture with hemorrhage RGO:08539 RGO:08544 paranasal sinus mass RGO:08544 RGO:08548 fracture with hematoma RGO:08548 SNOMEDCT:257548002 SNOMEDCT:44532001 RGO:08557 barotrauma RGO:08557 RGO:08560 epithelial papilloma RGO:08560 LCH histiocytosis X ORDO:389 RADLEX:RID3846 SNOMEDCT:128809007 SNOMEDCT:65399007 RGO:08562 Langerhans cell histiocytosis RGO:08562 SNOMEDCT:109361004 RGO:08568 surgical ciliated cyst RGO:08568 RGO:08569 fluid-filled sinus mass RGO:08569 HP:0000255 ICD10CM:J01 SNOMEDCT:15805002 RGO:08570 acute sinusitis RGO:08570 HP:0006888 SNOMEDCT:52330001 RGO:08573 meningoencephalocele RGO:08573 RGO:08574 necrotic malignant tumor RGO:08574 RGO:08575 sinus disease with bone destruction RGO:08575 SNOMEDCT:61011009 RGO:08577 bacterial osteomyelitis RGO:08577 Nocardia infection DOID:2312 ICD10CM:A43 ORDO:31204 SNOMEDCT:29227009 RGO:08579 nocardiosis RGO:08579 RGO:08581 idiopathic midline granuloma RGO:08581 RGO:08585 trauma with fracture RGO:08585 RGO:08586 temporomandibular joint disease RGO:08586 AS Bechterew disease Marie-Strümpell disease DOID:7147 ICD10CM:M45 RADLEX:RID3604 SNOMEDCT:9631008 RGO:08592 ankylosing spondylitis RGO:08592 DOID:813 RADLEX:RID3614 RGO:08596 infectious arthritis RGO:08596 RADLEX:RID5367 SNOMEDCT:20456003 RGO:08597 loose body RGO:08597 PVNS PVS DOID:2702 ORDO:66627 RADLEX:RID3641 SNOMEDCT:703703002 SNOMEDCT:95412009 RGO:08600 pigmented villonodular synovitis RGO:08600 DOID:9008 RADLEX:RID3554 SNOMEDCT:156370009 RGO:08601 psoriatic arthritis RGO:08601 RADLEX:RID13212 RGO:08603 normal variant RGO:08603 SNOMEDCT:442191000124102 RGO:08605 edentulous mandible RGO:08605 DOID:4959 ICD10CM:Q81.2 ORDO:303 SNOMEDCT:254185007 RGO:08606 epidermolysis bullosa dystrophica RGO:08606 SNOMEDCT:72855002 RGO:08609 congenital prognathism RGO:08609 mucolipidosis type III pseudo-Hurler polydystrophy pseudopolydystrophy ORDO:577 RGO:08613 mucolipidosis type 3 RGO:08613 RGO:08614 bilateral enlargement of the mandible in a child RGO:08614 small mandible HP:0000347 SNOMEDCT:32958008 RGO:08617 micrognathia RGO:08617 HP:0002804 SNOMEDCT:111246005 RGO:08621 arthrogryposis RGO:08621 DOID:0050648 SNOMEDCT:43814000 RGO:08622 atelosteogenesis RGO:08622 ORDO:1388 RGO:08624 Catel-Manzke syndrome RGO:08624 CCM syndrome cerebrocostomandibular syndrome ORDO:1393 SNOMEDCT:51780007 RGO:08625 cerebro-costo-mandibular syndrome RGO:08625 chromosome 18p- syndrome RGO:08627 chromosome 18:del(18p) syndrome RGO:08627 RGO:08628 contractural arachnodactyly RGO:08628 DOID:0060471 ORDO:1906 SNOMEDCT:17231009 RGO:08631 fetal valproate syndrome RGO:08631 DOID:14787 ORDO:2059 SNOMEDCT:702432006 RGO:08632 Fryns syndrome RGO:08632 RGO:08638 osteolysis with nephropathy RGO:08638 RGO:08651 congenital midface hypoplasia RGO:08651 Bloom-German syndrome DOID:2717 ORDO:125 SNOMEDCT:4434006 RGO:08653 Bloom syndrome RGO:08653 kyphomelic dysplasia several forms ORDO:1801 SNOMEDCT:254096001 RGO:08655 kyphomelic dysplasia RGO:08655 DOID:0050775 HP:0031026 ORDO:3144 SNOMEDCT:254049009 RGO:08656 Schneckenbecken dysplasia RGO:08656 SPOndylar and NAsal changes with STRIations of the MEtaphyses DOID:5684 ORDO:93357 SNOMEDCT:389161008 RGO:08657 SPONASTRIME dysplasia RGO:08657 delayed dental eruption delayed eruption HP:0000684 SNOMEDCT:5639000 RGO:08660 delayed tooth eruption RGO:08660 RADLEX:RID5663 SNOMEDCT:278923009 RGO:08664 developmental RGO:08664 DOID:2187 HP:0000705 ICD10CM:K00.5 ORDO:88661 SNOMEDCT:78494001 RGO:08665 amelogenesis imperfecta RGO:08665 iatrogenic effect RGO:08666 iatrogenesis RGO:08666 RGO:08669 nonodontogenic jaw lesion RGO:08669 HP:0100612 RADLEX:RID4178 SNOMEDCT:3833004 RGO:08671 odontogenic tumor RGO:08671 DOID:14793 HP:0007607 ORDO:238468 ORDO:248 SNOMEDCT:7731005 RGO:08676 hypohidrotic ectodermal dysplasia RGO:08676 cleidocranial dysplasia ORDO:1452 RGO:08684 cleidocranial dysostosis RGO:08684 Gorlin-Goltz syndrome NBCCS basal cell nevus syndrome multiple basal cell carcinoma syndrome nevoid basal cell carcinoma syndrome DOID:2512 ORDO:377 SNOMEDCT:69408002 RGO:08686 Gorlin syndrome RGO:08686 DOID:14213 ICD10CM:E83.39 ORDO:436 SNOMEDCT:190859005 RGO:08689 hypophosphatasia RGO:08689 MPS DOID:12798 RADLEX:RID34619 SNOMEDCT:11380006 RGO:08693 mucopolysaccharidosis RGO:08693 Albers-Schönberg disease DOID:13533 HP:0011002 ICD10CM:Q78.2 RADLEX:RID5392 SNOMEDCT:1926006 RGO:08695 osteopetrosis RGO:08695 Hutchinson-Gilford syndrome DOID:3911 ICD10CM:E34.8 SNOMEDCT:238870004 RGO:08696 progeria RGO:08696 pycnodysostosis SNOMEDCT:89647000 RGO:08697 pyknodysostosis RGO:08697 DOID:0050577 ORDO:1515 SNOMEDCT:254093009 RGO:08706 cranioectodermal dysplasia RGO:08706 craniofacial dysostosis DOID:2339 HP:0004439 ORDO:207 SNOMEDCT:28861008 RGO:08707 Crouzon syndrome RGO:08707 RGO:08708 DOOR syndrome RGO:08708 ORDO:1826 SNOMEDCT:62803002 RGO:08713 frontometaphyseal dysplasia RGO:08713 focal dermal hypoplasia DOID:2120 SNOMEDCT:2298005 RGO:08715 Goltz syndrome RGO:08715 oculo-mandibulo-facial syndrome DOID:4534 ORDO:2108 SNOMEDCT:7903009 RGO:08717 Hallermann-Streiff syndrome RGO:08717 SNOMEDCT:35031005 RGO:08718 Hanhart syndrome RGO:08718 aglossia-adactylia syndrome hypoglossia-hypodactylia syndrome ORDO:989 RGO:08720 hypoglossia-hypodactyly RGO:08720 incontinentia pigmenti achromians DOID:3156 ORDO:435 SNOMEDCT:218358001 RGO:08721 hypomelanosis of Ito RGO:08721 Bloch-Sulzberger syndrome ICD10CM:Q82.3 ORDO:464 RGO:08722 incontinentia pigmenti RGO:08722 DOID:14694 ORDO:2315 SNOMEDCT:75979009 RGO:08723 Johanson-Blizzard syndrome RGO:08723 DOID:14780 ORDO:2332 SNOMEDCT:711156009 RGO:08724 KBG syndrome RGO:08724 RGO:08725 Kocher-Debré-Sémélaigne syndrome RGO:08725 LADD syndrome Levy-Hollister syndrome lacrimoauriculodentodigital syndrome ORDO:2363 SNOMEDCT:23817003 RGO:08726 lacrimo-auriculo-dento-digital syndrome RGO:08726 DOID:0080195 ORDO:559 SNOMEDCT:80734006 RGO:08728 Marinesco-Sjögren syndrome RGO:08728 PFAPA syndrome ORDO:560 SNOMEDCT:33410002 RGO:08729 Marshall syndrome RGO:08729 Goldenhar syndrome OAV syndrome oculo-auricular-vertebral spectrum oculo-auricular-vertebral syndrome oculoauriculovertebral spectrum ORDO:141132 RGO:08731 oculo-auriculo-vertebral spectrum RGO:08731 oculodentoosseous dysplasia RGO:08732 oculo-dento-osseous dysplasia RGO:08732 OFD1 Papillon-Leage and Psaume syndrome Papillon-Leage-Psaume syndrome oral-facial-digital syndrome type 1 RGO:08733 orofaciodigital syndrome type 1 RGO:08733 osteoglophonic dwarfism SNOMEDCT:254144002 RGO:08736 osteoglophonic dysplasia RGO:08736 ORDO:85195 SNOMEDCT:254153009 RGO:08737 familial expansile osteolysis RGO:08737 DOID:0050449 ORDO:2309 SNOMEDCT:39427000 RGO:08739 pachyonychia congenita RGO:08739 juvenile periodontosis ORDO:678 SNOMEDCT:40158001 RGO:08740 Papillon-Lefèvre syndrome RGO:08740 DOID:11983 ICD10CM:Q87.1 ORDO:739 SNOMEDCT:89392001 RGO:08741 Prader-Willi syndrome RGO:08741 Robinow mesomelic dysplasia DOID:0060254 ORDO:97360 SNOMEDCT:76520005 RGO:08743 Robinow syndrome RGO:08743 Parry-Romberg syndrome hemifacial atrophy progressive hemifacial atrophy SNOMEDCT:718224004 RGO:08744 Romberg syndrome RGO:08744 poikiloderma congenitale DOID:2732 ORDO:2909 SNOMEDCT:69093006 RGO:08745 Rothmund-Thomson syndrome RGO:08745 Virchow-Seckel dwarfism bird-headed dwarfism DOID:0050569 ICD10CM:Q87.1 ORDO:808 SNOMEDCT:57917004 RGO:08746 Seckel syndrome RGO:08746 DOID:14501 ORDO:816 SNOMEDCT:111303009 RGO:08749 Sjögren-Larsson syndrome RGO:08749 arthro-ophthalmopathy DOID:0080046 ORDO:828 SNOMEDCT:78675000 RGO:08751 Stickler syndrome RGO:08751 Weyer acrofacial acrodental dysostosis RGO:08756 Weyers acrodental dysostosis RGO:08756 Torg-Winchester syndrome ORDO:3460 SNOMEDCT:254151006 RGO:08759 Winchester syndrome RGO:08759 49,XXXXY syndrome XXXXY disease chromosome XXXXY syndrome ORDO:96264 SNOMEDCT:38847009 RGO:08760 XXXXY syndrome RGO:08760 RGO:08762 early loss of teeth RGO:08762 DOID:1474 SNOMEDCT:49965002 RGO:08764 juvenile periodontitis RGO:08764 HP:0040289 ICD10CM:D70.4 ORDO:2686 RGO:08767 cyclic neutropenia RGO:08767 trichodentoosseous syndrome ORDO:3352 SNOMEDCT:38993008 RGO:08771 tricho-dento-osseous syndrome RGO:08771 congenital missing teeth RGO:08772 congenital hypodontia RGO:08772 Albright hereditary osteodystrophy DOID:4184 HP:0000852 ICD10CM:E20.1 ORDO:79443 SNOMEDCT:58976002 RGO:08773 pseudohypoparathyroidism RGO:08773 EECUT syndrome Rüdiger syndrome ectrodactyly - ectodermal dysplasia - cleft palate syndrome split hand - split foot - ectodermal dysplasia - cleft syndrome DOID:0060782 ORDO:1896 SNOMEDCT:39788007 RGO:08775 EEC syndrome RGO:08775 Mohr syndrome OFD2 RGO:08778 orofaciodigital syndrome type 2 RGO:08778 supernumerary teeth HP:0011069 SNOMEDCT:8666004 RGO:08780 hyperdontia RGO:08780 RGO:08782 loss of lamina dura of teeth RGO:08782 DOID:9893 ICD10CM:K05.4 SNOMEDCT:49965002 RGO:08786 periodontosis RGO:08786 RGO:08794 removal of opposing tooth RGO:08794 RGO:08801 agranulocytosis and cyclic neutropenia RGO:08801 Gorlin cyst RGO:08802 calcifying odontogenic keratocyst RGO:08802 RGO:08803 carcinoma of mouth RGO:08803 RADLEX:RID4295 SNOMEDCT:6842002 RGO:08804 desmoplastic fibroma RGO:08804 RGO:08811 mandibular periostitis RGO:08811 RGO:08815 reactive periostitis to adjacent soft tissue infection RGO:08815 RGO:08821 generalized osteopenia or osteolysis of the jaws RGO:08821 RGO:08833 cyclic neutropenia and agranulocytosis RGO:08833 RGO:08836 hypovitaminosis C RGO:08836 Gorham disease Gorham vanishing bone disease DOID:4837 SNOMEDCT:1515008 RGO:08837 massive osteolysis RGO:08837 RADLEX:RID9557 SNOMEDCT:15924003 SNOMEDCT:181204007 RGO:08844 maxillary sinus RGO:08844 RGO:08864 nonodontogenic radiolucent jaw lesion RGO:08864 GCT DOID:200 RADLEX:RID4309 SNOMEDCT:115238001 SNOMEDCT:443790001 RGO:08870 giant cell tumor RGO:08870 RGO:08876 cystic jaw lesion RGO:08876 RADLEX:RID4184 SNOMEDCT:27092008 RGO:08883 ameloblastic fibrosarcoma RGO:08883 Pindborg tumor SNOMEDCT:83048004 RGO:08885 calcifying epithelial odontogenic tumor RGO:08885 SNOMEDCT:88686005 RGO:08893 odontogenic fibroma RGO:08893 RADLEX:RID4203 SNOMEDCT:34941004 RGO:08895 odontogenic myxoma RGO:08895 RADLEX:RID4196 SNOMEDCT:28733007 RGO:08896 compound odontoma RGO:08896 RGO:08899 unilocular cystic jaw lesion RGO:08899 ICD10CM:K04.8 SNOMEDCT:89988002 RGO:08901 radicular cyst RGO:08901 SNOMEDCT:109608003 RGO:08902 residual cyst RGO:08902 RGO:08904 traumatic cyst RGO:08904 RGO:08905 multilocular jaw lesion RGO:08905 RADLEX:RID4183 SNOMEDCT:11063000 RGO:08907 ameloblastic fibroma RGO:08907 DOID:163 RGO:08908 mucoepidermoid tumor RGO:08908 RGO:08910 cystic lesion in maxilla RGO:08910 RGO:08911 cystic ameloblastoma RGO:08911 RGO:08916 simple unicameral bone cyst RGO:08916 RGO:08918 periapical radiolucency in jaw RGO:08918 RGO:08924 pulpoperiapical disease RGO:08924 RGO:08925 ameloblastic variant RGO:08925 RGO:08926 buccal cyst RGO:08926 RGO:08929 central odontogenic fibroma WHO type RGO:08929 DOID:701 HP:0011060 ORDO:1653 SNOMEDCT:109492001 RGO:08930 dentin dysplasia RGO:08930 RADLEX:RID4009 SNOMEDCT:278388008 RGO:08931 juvenile ossifying fibroma RGO:08931 RGO:08933 pseudotumor of hemophilia RGO:08933 RGO:08934 pericoronal radiolucency in the jaw RGO:08934 SNOMEDCT:89988002 RGO:08943 paradental cyst RGO:08943 RGO:08946 interradicular radiolucency in the jaw RGO:08946 SNOMEDCT:24140005 RGO:08956 median mandibular cyst RGO:08956 ICD10CM:K05.21 SNOMEDCT:83412009 RGO:08960 periodontal abscess RGO:08960 RGO:08961 periodontal bony pocket RGO:08961 RGO:08964 cyst-like mandibular lesion RGO:08964 RGO:08973 central squamous cell carcinoma in cyst lining RGO:08973 RGO:08976 minor salivary gland tumor in bone RGO:08976 RGO:08979 early odontoma RGO:08979 RGO:08980 postoperative maxillary cyst RGO:08980 RGO:08982 multiple well-defined radiolucent jaw lesions RGO:08982 SNOMEDCT:128462008 RGO:08985 metastases RGO:08985 RGO:08986 periapical granulomas RGO:08986 DOID:0050894 ORDO:314419 RADLEX:RID4187 SNOMEDCT:20462008 RGO:08987 ameloblastoma RGO:08987 brown tumor SNOMEDCT:203471008 RGO:08988 brown tumor of hyperparathyroidism RGO:08988 RGO:08990 giant cell granulomas RGO:08990 RADLEX:RID4209 SNOMEDCT:9155002 RGO:08996 squamous odontogenic tumor RGO:08996 RGO:08998 well-defined expansile radiolucent jaw lesion RGO:08998 SNOMEDCT:84983008 RGO:09002 ameloblastic odontoma RGO:09002 HP:0012062 RADLEX:RID3894 SNOMEDCT:203465002 SNOMEDCT:66954000 RGO:09004 bone cyst RGO:09004 RGO:09006 cementoossifying fibroma RGO:09006 MNTI melanotic progonoma neuroectodermal tumor of infancy SNOMEDCT:253076000 RGO:09007 melanotic neuroectodermal tumor of infancy RGO:09007 RGO:09011 ill-defined expansile radiolucent jaw lesion RGO:09011 RGO:09013 ill-defined lytic jaw lesion RGO:09013 RGO:09021 hematopoietic bone marrow defect RGO:09021 RGO:09023 malignant minor salivary gland tumor RGO:09023 SNOMEDCT:26888009 RGO:09025 odontogenic sarcoma RGO:09025 RGO:09028 lytic jaw lesion with internal residual bone RGO:09028 RGO:09029 invasive squamous cell carcinoma RGO:09029 RGO:09031 periapical mixed-radiopacity jaw lesion RGO:09031 RGO:09032 calcifying crown of developing tooth RGO:09032 RGO:09033 periapical cementoosseous dysplasia RGO:09033 RGO:09034 rarefying and condensing osteitis RGO:09034 RGO:09035 tooth root with rarefying osteitis RGO:09035 RGO:09041 pericoronal mixed-radiopacity jaw lesion RGO:09041 RGO:09042 ameloblastic fibroodontoma RGO:09042 RADLEX:RID4182 SNOMEDCT:6437002 RGO:09044 ameloblastic fibrodentinoma RGO:09044 RGO:09045 calcifying hyperplastic dental follicle RGO:09045 RGO:09046 cystic odontoma RGO:09046 RGO:09047 postsurgical healing RGO:09047 RGO:09048 mixed-radiopacity jaw lesion RGO:09048 SNOMEDCT:278401004 RGO:09051 desmoplastic ameloblastoma RGO:09051 RGO:09052 ossifying postsurgical bone defect RGO:09052 RGO:09053 ossifying subperiosteal hematoma RGO:09053 RADLEX:RID4191 SNOMEDCT:23255001 RGO:09060 cementoblastoma RGO:09060 RGO:09062 odontodysplasia RGO:09062 HP:0030433 RADLEX:RID4005 SNOMEDCT:302859004 SNOMEDCT:71666005 RGO:09064 osteoid osteoma RGO:09064 RGO:09067 solitary opacity in jaw RGO:09067 RADLEX:RID4195 SNOMEDCT:29020002 RGO:09069 complex odontoma RGO:09069 RGO:09071 idiopathic osteosclerosis RGO:09071 RGO:09073 retained tooth root RGO:09073 RGO:09078 dental periapical opacity RGO:09078 DOID:12733 ICD10CM:K03.4 SNOMEDCT:78537008 RGO:09080 hypercementosis RGO:09080 RGO:09086 multiple opaque jaw lesions RGO:09086 RGO:09088 multiple hypercementoses RGO:09088 RGO:09089 multiple periapical condensing osteitis RGO:09089 RGO:09091 multiple socket sclerosis RGO:09091 RGO:09095 familial gigantiform cementomas RGO:09095 HP:0011068 RGO:09098 multiple odontomas RGO:09098 RGO:09103 salivary gland abnormality RGO:09103 RGO:09106 salivary duct stricture on sialography RGO:09106 RADLEX:RID4994 SNOMEDCT:384600008 SNOMEDCT:56381008 RGO:09108 stone RGO:09108 SNOMEDCT:45338009 RGO:09110 salivary gland enlargement RGO:09110 DOID:10264 ICD10CM:B26 SNOMEDCT:36989005 RGO:09111 mumps RGO:09111 RADLEX:RID3661 SNOMEDCT:431501000124109 RGO:09130 sialodochitis fibrinosa RGO:09130 HP:0100684 RGO:09133 salivary gland neoplasm RGO:09133 SNOMEDCT:83472001 RGO:09139 acinic cell tumor RGO:09139 RGO:09142 cystic salivary gland mass RGO:09142 RGO:09143 cystic lymphoma RGO:09143 RADLEX:RID3937 SNOMEDCT:69825009 RGO:09149 sialocele RGO:09149 adenolymphoma monomorphic adenoma papillary cystadenoma lymphomatosum RADLEX:RID4238 RGO:09150 Warthin tumor RGO:09150 RGO:09151 multiple discrete intraparotid lesions RGO:09151 RGO:09153 multicentric oncocytoma RGO:09153 RGO:09154 multicentric Warthin tumors RGO:09154 RGO:09156 multiple branchial cleft cysts RGO:09156 RGO:09157 multiple intraparotid cysts RGO:09157 RGO:09158 multiple pleomorphic adenomas RGO:09158 RGO:09159 bilaterally enlarged and heterogeneous parotids RGO:09159 SNOMEDCT:66590003 RGO:09161 chronic alcoholism RGO:09161 HP:0003077 RADLEX:RID39096 SNOMEDCT:55822004 RGO:09162 hyperlipidemia RGO:09162 DOID:5389 RADLEX:RID4515 SNOMEDCT:89439007 RGO:09169 oncocytoma RGO:09169 RGO:09173 clear cell oncocytosis RGO:09173 dysgenetic parotid disease RGO:09174 polycystic parotid disease RGO:09174 RGO:09175 small parotid gland RGO:09175 RGO:09176 chronic postobstructive atrophy RGO:09176 RGO:09178 bilateral cheek masses RGO:09178 RGO:09180 bilateral accessory parotid gland tissue RGO:09180 RGO:09181 bilateral facial processes of the parotid glands RGO:09181 RGO:09184 viral parotitis RGO:09184 RGO:09187 alcohol-related parotid gland hypertrophy RGO:09187 RGO:09188 submandibular space lesion RGO:09188 SNOMEDCT:92415001 RGO:09189 benign tumor of submandibular gland RGO:09189 DOID:1475 HP:0100764 RADLEX:RID4370 SNOMEDCT:400178008 SNOMEDCT:69044001 RGO:09194 lymphangioma RGO:09194 RGO:09195 pseudotumor secondary to motor atrophy of cranial nerve RGO:09195 DOID:12904 HP:0030706 ICD10CM:K11.6 RADLEX:RID3919 SNOMEDCT:14919007 RGO:09196 ranula RGO:09196 HP:0010518 ORDO:489 RADLEX:RID3943 SNOMEDCT:39462005 RGO:09197 thyroglossal duct cyst RGO:09197 RGO:09198 sublingual space lesion RGO:09198 RGO:09201 dilated excretory duct of submandibular gland RGO:09201 RGO:09202 hypoglossal nerve atrophy RGO:09202 HP:0100029 RADLEX:RID3770 SNOMEDCT:129123002 SNOMEDCT:21279007 RGO:09203 lingual thyroid RGO:09203 RGO:09205 soft-tissue neck mass RGO:09205 RGO:09210 cervical thymic cyst RGO:09210 SNOMEDCT:190459003 RGO:09216 parathyroid cyst RGO:09216 DOID:11074 RGO:09218 thyroid cyst RGO:09218 RGO:09221 cervical thymus gland RGO:09221 DOID:3350 RGO:09225 mesenchymal tumor RGO:09225 DOID:7608 HP:0002897 SNOMEDCT:128474007 RGO:09227 parathyroid adenoma RGO:09227 HP:0200040 ICD10CM:L72.3 SNOMEDCT:417992006 SNOMEDCT:419603000 RGO:09228 sebaceous cyst RGO:09228 RGO:09232 dilated jugular lymph sac RGO:09232 RGO:09235 posttraumatic pseudoaneurysm RGO:09235 RGO:09239 internal jugular vein thrombosis RGO:09239 RGO:09248 metastatic cervical lymphadenopathy RGO:09248 RGO:09267 solid mass in carotid sheath RGO:09267 SNOMEDCT:230650009 SNOMEDCT:63561003 RGO:09269 traumatic neuroma RGO:09269 RGO:09272 thyroid lesion RGO:09272 RGO:09279 ill-defined enlarged thyroid with extrathyroid extension RGO:09279 RGO:09288 fatty tumor of the neck RGO:09288 RGO:09293 diffuse lipomatosis of the neck RGO:09293 DOID:11981 SNOMEDCT:238136002 RGO:09297 morbid obesity RGO:09297 ORDO:199276 RGO:09298 multiple familial lipomatosis RGO:09298 RGO:09301 progressive nodular lipomatosis RGO:09301 DOID:1525 SNOMEDCT:33760009 RGO:09302 Weber-Christian disease RGO:09302 increased retropharyngeal space in infants or children RGO:09303 increased prevertebral space in infants or children RGO:09303 RGO:09312 lymph fluid RGO:09312 RGO:09316 retropharyngeal goiter RGO:09316 increased retropharyngeal space in an adult RGO:09320 increased prevertebral space in an adult RGO:09320 RGO:09324 postcricoid carcinoma RGO:09324 SNOMEDCT:401051003 RGO:09326 tortuous carotid artery RGO:09326 SNOMEDCT:33431000119109 RGO:09329 oropharyngeal lesion RGO:09329 RGO:09341 chromosome 4:dup(4p) syndrome RGO:09341 RGO:09344 jaw or dental deformity with increased mouth size RGO:09344 RGO:09350 base of tongue mass RGO:09350 RGO:09354 cystic floor-of-mouth mass RGO:09354 RGO:09357 necrotic neoplasm RGO:09357 RGO:09360 lesions of the hypopharynx, larynx, and upper trachea RGO:09360 RGO:09367 juvenile papillomatosis RGO:09367 SNOMEDCT:18099001 RGO:09370 retropharyngeal abscess RGO:09370 RGO:09375 midline granuloma RGO:09375 SNOMEDCT:1416000100000410 RGO:09376 vallecular mass RGO:09376 ICD10CM:Q31.3 ORDO:2372 RADLEX:RID4821 SNOMEDCT:51523009 RGO:09378 laryngocele RGO:09378 RGO:09379 tongue base cyst RGO:09379 SNOMEDCT:232410007 RGO:09380 vallecular cyst RGO:09380 HP:0100028 RGO:09382 ectopic thyroid RGO:09382 RGO:09383 pyriform sinus mass RGO:09383 RGO:09384 carcinoma of pyriform sinus RGO:09384 RGO:09385 postradiation edema RGO:09385 RGO:09386 enlarged epiglottis RGO:09386 RGO:09390 congenital aryepiglottic enlargement RGO:09390 RGO:09391 congenital omega epiglottis RGO:09391 RADLEX:RID3936 SNOMEDCT:367645008 RGO:09398 retention cyst RGO:09398 RGO:09399 supraglottic mass RGO:09399 RGO:09402 paralaryngeal cystic mass RGO:09402 ORDO:141124 RGO:09403 congenital laryngeal cyst RGO:09403 RGO:09406 laryngeal asymmetry RGO:09406 RGO:09407 arytenoid dislocation RGO:09407 RGO:09408 recurrent laryngeal nerve paralysis RGO:09408 RGO:09409 superior laryngeal nerve paralysis RGO:09409 RGO:09410 traumatic deformity RGO:09410 RGO:09411 abnormal laryngeal cartilage RGO:09411 SNOMEDCT:276655000 SNOMEDCT:385297003 RGO:09413 congenital deformity RGO:09413 DOID:2598 RGO:09417 laryngeal tumor RGO:09417 RGO:09423 vocal cord asymmetry RGO:09423 RGO:09425 papilloma of vocal cord RGO:09425 RGO:09426 teflon injection of vocal cord RGO:09426 RGO:09427 vocal cord paralysis or paresis RGO:09427 SNOMEDCT:254638002 RGO:09433 superior sulcus tumor RGO:09433 DOID:6111 RGO:09437 jugular foramen neoplasm RGO:09437 RGO:09438 subglottic tracheal narrowing RGO:09438 hyalinosis cutis DOID:14498 ORDO:530 SNOMEDCT:38692000 RGO:09450 lipoid proteinosis RGO:09450 RGO:09452 upper airway obstruction in a child RGO:09452 DOID:4558 SNOMEDCT:196542004 RGO:09458 Ludwig angina RGO:09458 RGO:09461 tonsil and adenoid hypertrophy RGO:09461 DOID:2615 SNOMEDCT:82049002 RGO:09468 papillomatosis RGO:09468 RGO:09471 congenital vertebral abnormality RGO:09471 DOID:14687 ICD10CM:Q77.5 ORDO:628 RADLEX:RID34680 SNOMEDCT:58561002 RGO:09475 diastrophic dysplasia RGO:09475 DOID:0050665 ORDO:1915 SNOMEDCT:205788004 RGO:09477 fetal alcohol syndrome RGO:09477 HOS atrio-digital syndrome atriodigital dysplasia cardiac-limb syndrome heart-hand syndrome type 1 ventriculo-radial syndrome DOID:0060468 ICD10CM:Q87.2 ORDO:392 SNOMEDCT:19092004 RGO:09478 Holt-Oram syndrome RGO:09478 DOID:9263 HP:0002156 ICD10CM:E72.11 ORDO:394 SNOMEDCT:11282001 RGO:09479 homocystinuria RGO:09479 Fairbank syndrome DOID:12721 HP:0002654 ORDO:251 SNOMEDCT:59708000 RGO:09485 multiple epiphyseal dysplasia RGO:09485 NF DOID:8712 HP:0001067 RADLEX:RID34599 SNOMEDCT:81669005 RGO:09486 neurofibromatosis RGO:09486 DOID:3490 ICD10CM:Q87.1 ORDO:648 SNOMEDCT:205824006 RGO:09487 Noonan syndrome RGO:09487 Ekman-Lobstein syndrome OI Vrolik syndrome glass-bone disease DOID:12347 ICD10CM:Q78.0 ORDO:666 RADLEX:RID34746 SNOMEDCT:78314001 RGO:09488 osteogenesis imperfecta RGO:09488 pseudoachondroplastic spondyloepiphyseal dysplasia DOID:0080047 ORDO:750 SNOMEDCT:22567005 RGO:09490 pseudoachondroplasia RGO:09490 DOID:0050813 HP:0002655 ICD10CM:Q77.7 SNOMEDCT:278713008 RGO:09491 spondyloepiphyseal dysplasia RGO:09491 SMD HP:0002657 RGO:09492 spondylometaphyseal dysplasia RGO:09492 maxillonasal dysplasia nasomaxillovertebral syndrome DOID:14683 SNOMEDCT:715985008 RGO:09500 Binder syndrome RGO:09500 DOID:0050690 ORDO:1293 SNOMEDCT:254088006 RGO:09501 brachyolmia RGO:09501 DOID:11577 ICD10CM:G83.4 SNOMEDCT:192970008 RGO:09503 cauda equina syndrome RGO:09503 ichthyosis-limb reduction syndrome ORDO:139 SNOMEDCT:17608003 RGO:09505 CHILD syndrome RGO:09505 DOID:2962 ICD10CM:Q87.1 ORDO:191 RADLEX:RID5131 SNOMEDCT:21086008 RGO:09507 Cockayne syndrome RGO:09507 RGO:09514 dysspondylochondromatosis RGO:09514 Chernogubov syndrome EDS DOID:13359 ICD10CM:Q79.6 SNOMEDCT:398114001 RGO:09515 Ehlers-Danlos syndrome RGO:09515 femoral hypoplasia-unusual face syndrome RGO:09517 femoral hypoplasia-unusual facies syndrome RGO:09517 HP:0003155 RGO:09524 hyperphosphatasia RGO:09524 DOID:14764 SNOMEDCT:63387002 RGO:09528 Larsen syndrome RGO:09528 cardiocutaneous syndrome cardiomyopathic lentiginosis familial multiple lentigines syndrome lentiginosis profusa syndrome multiple lentigines syndrome progressive cardiomyopathic lentiginosis DOID:14291 ORDO:500 SNOMEDCT:111306001 RGO:09529 LEOPARD syndrome RGO:09529 Escobar syndrome autosomal dominant multiple pterygium syndrome distal arthrogryposis type 8 DOID:0080110 ORDO:65743 SNOMEDCT:205819008 RGO:09533 multiple pterygium syndrome RGO:09533 RGO:09536 oculovertebral syndrome RGO:09536 pseudoleprechaunism ORDO:2976 RGO:09541 Patterson syndrome RGO:09541 Pyle disease familial metaphyseal dysplasia metaphyseal dysplasia Pyle type ORDO:3005 RGO:09546 Pyle dysplasia RGO:09546 RGO:09553 shawl scrotum syndrome RGO:09553 DOID:2255 ORDO:1505 RGO:09554 short rib-polydactyly syndrome RGO:09554 spondylocarpotarsal synostosis syndrome RGO:09556 spondylocarpotarsal fusion syndrome RGO:09556 Jarcho-Levin syndrome spondylocostal dysplasia DOID:0050568 ORDO:2311 RGO:09557 spondylocostal dysostosis RGO:09557 SEMD DOID:0080027 HP:0002651 SNOMEDCT:254062008 RGO:09558 spondyloepimetaphyseal dysplasia RGO:09558 SNOMEDCT:702339001 RGO:09559 spondyloperipheral dysplasia RGO:09559 SNOMEDCT:70534000 RGO:09561 tethered cord syndrome RGO:09561 VATER syndrome SNOMEDCT:27742002 RGO:09564 VATER association RGO:09564 HP:0009800 RGO:09572 maternal diabetes RGO:09572 HP:0000912 ORDO:3181 RADLEX:RID4785 RGO:09573 Sprengel deformity RGO:09573 Halasz syndrome venolobar syndrome DOID:4297 HP:0011626 ICD10CM:Q26.8 ORDO:185 SNOMEDCT:39905002 RGO:09576 scimitar syndrome RGO:09576 osteonecrosis of the vertebral epiphysis DOID:13300 HP:0010891 RADLEX:RID5378 RGO:09588 Scheuermann disease RGO:09588 HP:0003324 RGO:09591 generalized weakness RGO:09591 RGO:09592 radiation therapy atrophy RGO:09592 HP:0002947 SNOMEDCT:298393001 RGO:09593 cervical kyphosis RGO:09593 HP:0002953 RADLEX:RID4658 SNOMEDCT:21947006 SNOMEDCT:443395009 RGO:09595 compression fracture RGO:09595 Desbuquois syndrome DOID:0060462 ORDO:1425 RGO:09596 Desbuquois dysplasia RGO:09596 ORDO:85174 SNOMEDCT:254058002 RGO:09599 pseudodiastrophic dysplasia RGO:09599 HP:0005619 RGO:09601 thoracolumbar gibbus RGO:09601 RGO:09603 pyogenic osteomyelitis RGO:09603 RGO:09604 severe Scheuermann disease RGO:09604 Pott disease ICD10CM:A18.01 RADLEX:RID3725 SNOMEDCT:35984006 RGO:09605 tuberculous spondylitis RGO:09605 RGO:09611 degenerative spondylosis RGO:09611 DOID:90 HP:0008419 RADLEX:RID5086 SNOMEDCT:77547008 RGO:09612 degenerative disc disease RGO:09612 RGO:09624 paraspinal soft-tissue mass RGO:09624 DOID:0050773 HP:0030074 SNOMEDCT:302834008 SNOMEDCT:51747000 RGO:09635 chemodectoma RGO:09635 correction for transposition of great vessels RGO:09641 Mustard procedure RGO:09641 SNOMEDCT:253867006 RGO:09648 thoracic kidney RGO:09648 RGO:09652 bilateral interfacetal dislocation of cervical spine RGO:09652 RGO:09653 clay-shoveler fracture RGO:09653 RGO:09654 flexion teardrop fracture of cervical spine RGO:09654 RGO:09655 simple wedge fracture of cervical spine RGO:09655 RGO:09657 rotatory dislocation of cervical spine with interlocking RGO:09657 RGO:09658 unilateral interfacetal dislocation or fracture-dislocation of cervical spine RGO:09658 RGO:09681 odontoid fracture RGO:09681 HP:0000473 ICD10CM:M43.6 RADLEX:RID4816 SNOMEDCT:70070008 RGO:09688 torticollis RGO:09688 HP:0003467 SNOMEDCT:202820009 RGO:09706 atlantoaxial instability RGO:09706 absent C1 anterior arch RGO:09712 absent anterior arch of atlas RGO:09712 RGO:09716 C2-C3 block vertebra RGO:09716 RGO:09720 congenital atlantoaxial subluxation or instability RGO:09720 abnormal dens HP:0003310 RGO:09729 abnormal odontoid process RGO:09729 MPS 4 mucopolysaccharidosis type 4 ICD10CM:E76.219 RADLEX:RID34618 SNOMEDCT:378007 RGO:09732 Morquio syndrome RGO:09732 calcinosis - Raynaud phenomenon - esophageal dysmotility - sclerodactyly - telangiectasia limited cutaneous form of systemic sclerosis DOID:0060218 ORDO:90290 SNOMEDCT:31848007 RGO:09735 CREST syndrome RGO:09735 RGO:09739 congenital craniovertebral junction abnormality RGO:09739 RGO:09741 asymmetric atlantoaxial joint RGO:09741 RGO:09742 asymmetric atlanto-occipital joint RGO:09742 RGO:09743 posterior arch of atlas defect RGO:09743 RGO:09744 C1 rachischisis RGO:09744 HP:0002677 SNOMEDCT:444879009 RGO:09750 stenosis of foramen magnum RGO:09750 RGO:09751 stenosis of cervical spinal canal RGO:09751 RGO:09755 acquired craniovertebral junction abnormality RGO:09755 SNOMEDCT:128139000 RGO:09757 inflammatory disease RGO:09757 cervical vertebral fusion fusion of cervical spine HP:0002949 RGO:09764 cervical spine fusion RGO:09764 ICD10CM:Q06.2 ORDO:1671 SNOMEDCT:49351009 RGO:09774 diastematomyelia RGO:09774 RGO:09775 isolated anomaly RGO:09775 RGO:09776 meningomyelocele with spinal dysraphism RGO:09776 ORDO:2578 RGO:09783 MURCS association RGO:09783 Poland anomaly Poland sequence pectoral muscle aplasia-syndactyly syndrome DOID:12961 ICD10CM:Q79.8 ORDO:2911 SNOMEDCT:38371006 RGO:09784 Poland syndrome RGO:09784 RGO:09785 split notochord syndrome RGO:09785 cervico-oculo-acoustic syndrome ORDO:3456 SNOMEDCT:79665007 RGO:09789 Wildervanck syndrome RGO:09789 RGO:09790 absent or minimally ossified vertebrae RGO:09790 DOID:0050680 ORDO:1263 SNOMEDCT:254054000 RGO:09791 boomerang dysplasia RGO:09791 spondylo-megaepiphyseal-metaphyseal dysplasia RGO:09793 spondylomegaepiphyseal-metaphyseal dysplasia RGO:09793 HP:0003417 RGO:09794 coronal cleft vertebrae RGO:09794 RGO:09798 malsegmentation of spine RGO:09798 RGO:09800 spondyloepimetaphyseal dysplasia Iraqi type RGO:09800 RGO:09801 Weissenbacher-Zweymüller phenotype RGO:09801 large central venous groove of a vertebral body RGO:09802 large anterior canal of a vertebral body RGO:09802 HP:0000926 RGO:09805 platyspondyly RGO:09805 RGO:09814 severe hypophosphatasia RGO:09814 lethal osteosclerotic bone dysplasia lethal sclerosing skeletal dysplasia ORDO:1832 RGO:09816 lethal osteosclerotic skeletal dysplasia RGO:09816 SNOMEDCT:389268008 RGO:09820 spondyloenchondromatosis RGO:09820 HP:0002879 RGO:09825 anisospondyly RGO:09825 RGO:09827 solitary collapsed vertebra RGO:09827 RGO:09838 multiple collapsed vertebrae RGO:09838 fish-mouth vertebra RGO:09845 biconcave vertebra RGO:09845 intraosseous herniation of disk RADLEX:RID35520 RADLEX:RID4939 RGO:09848 Schmorl node RGO:09848 RGO:09850 wedged vertebra RGO:09850 RGO:09859 anterior beaked vertebrae in a child RGO:09859 RGO:09866 adenosine deaminase deficiency with severe combined immunodeficiency and chondro-osseous dysplasia RGO:09866 RGO:09869 spondyloepimetaphyseal dysplasia short limb-hand type RGO:09869 RGO:09870 cuboid vertebrae RGO:09870 RGO:09873 round vertebrae RGO:09873 ORDO:3237 SNOMEDCT:62628008 RGO:09891 multiple synostosis syndrome RGO:09891 RGO:09896 surgical fusion RGO:09896 RGO:09898 enlarged vertebrae RGO:09898 RGO:09903 squaring of vertebral body RGO:09903 anterior and posterior vertebral scalloping RGO:09904 spool-shaped vertebrae RGO:09904 HP:0001290 SNOMEDCT:398152000 RGO:09905 hypotonia RGO:09905 RGO:09908 anterior vertebral scalloping RGO:09908 RADLEX:RID35455 RGO:09917 posterior vertebral scalloping RGO:09917 rugger jersey spine RGO:09927 dense subchondral zone of vertebra RGO:09927 RGO:09929 sclerosing spondylosis in the elderly RGO:09929 HP:0031164 RGO:09930 growth arrest lines RGO:09930 ORDO:2777 RGO:09936 osteomesopyknosis RGO:09936 sandwich vertebra RGO:09937 bone-in-bone vertebra RGO:09937 corduroy vertebral body pin-stripe vertebral body RGO:09942 vertical trabeculation of vertebral body RGO:09942 DOID:0080039 RGO:09944 axial osteomalacia RGO:09944 DOID:0080040 RGO:09945 fibrogenesis imperfecta ossium RGO:09945 focal sclerosis in vertebra RGO:09948 focal vertebral sclerosis RGO:09948 RGO:09950 sclerosis of apophyseal joint RGO:09950 RGO:09955 sclerotic pedicle RGO:09955 ivory vertebra RGO:09956 densely sclerotic vertebra RGO:09956 DOID:13068 ICD10CM:N25.0 SNOMEDCT:16726004 RGO:09960 renal osteodystrophy RGO:09960 RGO:09966 healing rickets RGO:09966 RGO:09967 spinal osteopenia RGO:09967 RGO:09973 lytic vertebral lesion RGO:09973 fibroxanthoma nonossifying fibromas RADLEX:RID4290 RGO:09982 nonossifying fibroma RGO:09982 RGO:09983 vertebral neoplasm RGO:09983 DOID:2705 RGO:09984 malignant giant cell tumor RGO:09984 RGO:09989 expansile bone lesion RGO:09989 RGO:09994 enlarged vertebral pedicle RGO:09994 RGO:09997 dysplastic vertebral pedicle RGO:09997 RGO:09999 flattened vertebral pedicle RGO:09999 RGO:10002 vertebral pedicle destruction RGO:10002 RGO:10009 vertebral pedicle sclerosis RGO:10009 RGO:10014 small intervertebral foramen RGO:10014 RGO:10017 posterior subluxation of cervical spine RGO:10017 RGO:10018 unilateral bar resulting in scoliosis RGO:10018 RGO:10019 enlarged intervertebral foramen RGO:10019 RGO:10025 fibroma of spinal ligaments RGO:10025 RGO:10026 lateral thoracic meningocele RGO:10026 RGO:10027 metastasis to spine or nerve RGO:10027 DOID:2300 HP:0003304 ICD10CM:M43.0 RADLEX:RID5120 SNOMEDCT:240221008 RGO:10032 spondylolysis RGO:10032 RGO:10034 congenital posterior neural arch defect RGO:10034 RGO:10039 acquired posterior neural arch defect RGO:10039 DOID:0080073 HP:0003298 ICD10CM:Q76.0 SNOMEDCT:76916001 RGO:10043 spina bifida occulta RGO:10043 SNOMEDCT:239151003 RGO:10045 dorsal dermal sinus RGO:10045 RGO:10046 filum terminate lipoma RGO:10046 HP:0030710 SNOMEDCT:253120005 RGO:10048 lipomeningocele RGO:10048 ORDO:268369 SNOMEDCT:58557008 RGO:10049 spina bifida aperta RGO:10049 SNOMEDCT:82058009 RGO:10050 myelocele RGO:10050 HP:0030708 SNOMEDCT:360530005 RGO:10051 myeloschisis RGO:10051 RGO:10052 sacral agenesis or hypoplasia RGO:10052 curved sacrum sickle-shaped sacrum RGO:10055 sacral deformity RGO:10055 ORDO:1552 SNOMEDCT:413936007 RGO:10056 Currarino triad RGO:10056 caudal appendage sacral appendage sacrococcygeal tail tail RGO:10059 sacrococcygeal appendage RGO:10059 RGO:10063 sacroiliac joint disease RGO:10063 SNOMEDCT:203489009 RGO:10065 osteitis condensans ilii RGO:10065 lipoid dermatoarthritis DOID:11824 ORDO:139436 SNOMEDCT:84241008 RGO:10072 multicentric reticulohistiocytosis RGO:10072 RGO:10075 sacroiliitis circumscripta RGO:10075 RGO:10076 symmetrical sacroiliac joint abnormality RGO:10076 DJD degenerative joint disease DOID:8398 HP:0002758 RADLEX:RID3555 SNOMEDCT:396275006 RGO:10078 osteoarthritis RGO:10078 MCTD DOID:3492 ICD10CM:M35.1 ORDO:809 SNOMEDCT:398049005 RGO:10080 mixed connective tissue disease RGO:10080 RGO:10081 asymmetrical sacroiliac joint abnormality RGO:10081 RGO:10082 unilateral sacroiliac joint abnormality RGO:10082 RGO:10084 presacral abscess RGO:10084 RGO:10096 neurogenic tumor RGO:10096 SNOMEDCT:712861006 RGO:10097 osteomyelitis of sacrum RGO:10097 ORDO:171220 RGO:10099 rectal duplication RGO:10099 RGO:10100 sacral neoplasm RGO:10100 RGO:10106 paget sarcoma RGO:10106 RGO:10107 radiation-induced sarcoma RGO:10107 RGO:10108 narrow intervertebral disk space RGO:10108 HP:0008441 RGO:10112 herniated disk RGO:10112 HP:0002655 ORDO:93284 SNOMEDCT:51952004 RGO:10120 spondyloepiphyseal dysplasia tarda RGO:10120 RGO:10121 wide intervertebral disk space RGO:10121 HP:0004586 RGO:10122 biconcave vertebrae RGO:10122 RGO:10123 calcific discitis RGO:10123 RGO:10127 tumor crossing an intervertebral disk RGO:10127 HP:0005645 SNOMEDCT:240211000 RGO:10128 intervertebral disk calcification RGO:10128 gas in intervertebral disk RADLEX:RID35679 RGO:10136 vacuum disk phenomenon RGO:10136 RGO:10140 fractured vertebra RGO:10140 congenital spinal stenosis ORDO:831 RGO:10143 congenital narrow spinal canal RGO:10143 RGO:10145 dyschondrosteosis RGO:10145 distal arthrogryposis type 3 ORDO:376 SNOMEDCT:237850008 RGO:10146 Gordon syndrome RGO:10146 RGO:10153 frontometaphysea RGO:10153 RGO:10156 intramedullary spinal lesion RGO:10156 RGO:10168 postradiation myelopathy RGO:10168 RGO:10169 spinal cord atrophy RGO:10169 SNOMEDCT:262710003 RGO:10170 transection of spinal cord RGO:10170 RGO:10175 ischemia with cord infarction RGO:10175 SNOMEDCT:60576007 RGO:10177 subacute combined degeneration RGO:10177 RGO:10178 intradural extramedullary spinal lesion RGO:10178 DOID:12156 ORDO:137817 RADLEX:RID3496 SNOMEDCT:8217007 RGO:10179 arachnoiditis RGO:10179 RGO:10182 ependymoma of filum terminale RGO:10182 RGO:10185 tortuosity of nerve roots RGO:10185 RGO:10187 pantopaque myelography RGO:10187 RGO:10188 spinal meningitis RGO:10188 RGO:10189 extradural spinal lesion RGO:10189 RGO:10191 epidural metastasis RGO:10191 RGO:10197 extradural spinal lipomatosis RGO:10197 RGO:10204 epidural granuloma RGO:10204 SNOMEDCT:231249005 RGO:10208 spinal block RGO:10208 RGO:10210 intervertebral joint disorder RGO:10210 DOID:6725 HP:0003416 ICD10CM:M48.0 RADLEX:RID5028 SNOMEDCT:76107001 RGO:10214 spinal stenosis RGO:10214 RGO:10218 vertebral hemangioma RGO:10218 RGO:10220 lipoma of canal RGO:10220 RGO:10221 osteomyelitis of spine RGO:10221 RGO:10222 tortuous myelographic filling defect RGO:10222 RGO:10227 sclerosing bone dysplasia RGO:10227 DOID:11991 HP:0010739 ICD10CM:Q78.8 SNOMEDCT:9147009 RGO:10230 osteopoikilosis RGO:10230 Sedaghatian type spondylometaphyseal dysplasia ORDO:93317 RGO:10264 spondylometaphyseal dysplasia Sedaghatian type RGO:10264 RGO:10265 late-onset dwarfism RGO:10265 HP:0008905 RGO:10273 rhizomelic dwarfism RGO:10273 DOID:0060288 ORDO:2733 RGO:10275 omodysplasia RGO:10275 enchondromatosis with severe platyspondyly ORDO:1855 SNOMEDCT:254079002 RGO:10276 spondyloenchondrodysplasia RGO:10276 HP:0008845 RGO:10277 mesomelic dwarfism RGO:10277 achondrogenesis Brazilian type nonlethal achondrogenesis DOID:0080052 RGO:10282 Grebe chondrodysplasia RGO:10282 RGO:10285 acromelic dwarfism RGO:10285 ORDO:969 SNOMEDCT:254090007 RGO:10286 acromicric dysplasia RGO:10286 RGO:10289 congenital short limbs RGO:10289 Mietens syndrome intellectual deficit Mietens-Weber type ORDO:2557 RGO:10298 Mietens-Weber syndrome RGO:10298 RGO:10299 spondyloepiphyseal dysplasias RGO:10299 RGO:10300 short squat bones RGO:10300 RGO:10306 bowed bones RGO:10306 OFC osteitis fibrosa osteodystrophia fibrosa von Recklinghausen disease of bone RADLEX:RID3525 SNOMEDCT:84727000 RGO:10310 osteitis fibrosa cystica RGO:10310 RGO:10314 prenatal bowing of long bones RGO:10314 SNOMEDCT:72687002 RGO:10320 congenital pseudoarthrosis RGO:10320 RGO:10323 intrauterine positional deformity RGO:10323 ORDO:198 SNOMEDCT:59399004 RGO:10327 occipital horn syndrome RGO:10327 ORDO:3344 RGO:10330 Weismann-Netter syndrome RGO:10330 RGO:10331 twisted bones RGO:10331 bone overconstriction bone overtubulation narrow diametaphysis RGO:10335 long thin bones RGO:10335 SNOMEDCT:240129002 RGO:10337 disuse atrophy RGO:10337 bone underconstriction bone undertubulation RGO:10345 wide diametaphysis RGO:10345 ORDO:2900 RGO:10357 Léri pleonosteosis RGO:10357 ballooned bones RGO:10360 broad tubular bones RGO:10360 RGO:10368 limb asymmetry RGO:10368 RGO:10376 lymphatic abnormality RGO:10376 RGO:10378 macrodystrophia lipomatosa RGO:10378 RGO:10394 localized bone overgrowth RGO:10394 RGO:10401 congenital macrodactyly RGO:10401 RGO:10409 familial tall stature RGO:10409 DOID:0060476 ORDO:2849 SNOMEDCT:302849000 RGO:10413 Perlman syndrome RGO:10413 RGO:10420 idiopathic isosexual precocious puberty RGO:10420 RGO:10424 exogenous obesity with overgrowth and tall stature RGO:10424 RGO:10441 small for gestational age neonate RGO:10441 RGO:10446 retarded skeletal maturation RGO:10446 DOID:0060857 HP:0100842 RGO:10450 de Morsier syndrome RGO:10450 ORDO:2044 SNOMEDCT:312214005 RGO:10451 floating-harbor syndrome RGO:10451 RGO:10452 infant of toxemic mother RGO:10452 pituitary dwarfism II DOID:9521 ORDO:633 RGO:10453 Laron syndrome RGO:10453 DOID:0110970 ORDO:93384 RGO:10462 brachydactyly type C RGO:10462 DOID:0060739 ORDO:2438 SNOMEDCT:702425002 RGO:10465 hand-foot-genital syndrome RGO:10465 RGO:10468 irregular epiphyseal ossification centers RGO:10468 RGO:10471 osteochondroses RGO:10471 RGO:10472 hypo-hyperparathyroidism RGO:10472 osteonecrosis of base of phalanx osteonecrosis of bases of phalanges RGO:10475 Thiemann disease RGO:10475 RGO:10476 vitamin K reductase deficiency RGO:10476 ORDO:168621 RGO:10487 Meyer dysplasia of the femoral head RGO:10487 ORDO:1952 RGO:10490 Pacman dysplasia RGO:10490 trichorhinophalangeal syndrome RGO:10491 trichorhinophalangeal dysplasia RGO:10491 epiphyseal stippling punctate epiphyseal calcification punctate epiphyses HP:0010655 SNOMEDCT:360507004 RGO:10492 stippled epiphyses RGO:10492 RGO:10493 multiple abnormal epiphyses RGO:10493 SNOMEDCT:161006 SNOMEDCT:713346006 RGO:10505 thermal injury RGO:10505 RGO:10509 hormone-secreting neoplasm causing precocious puberty RGO:10509 Voorhoeve disease HP:0010740 SNOMEDCT:82663009 RGO:10511 osteopathia striata RGO:10511 RGO:10512 generalized small epiphyses RGO:10512 RGO:10517 localized small epiphyses RGO:10517 RGO:10525 generalized large epiphyses RGO:10525 SNOMEDCT:239796000 RGO:10527 juvenile chronic arthritis RGO:10527 RGO:10529 spondyloepiphyseal dysplasia with macroepiphyses RGO:10529 RGO:10530 localized large epiphyses RGO:10530 RGO:10533 hemophilic hemarthrosis RGO:10533 RGO:10536 idiopathic localized gigantism RGO:10536 RGO:10541 thin epiphyses RGO:10541 fuzzy epiphyses RGO:10543 indistinct epiphyses RGO:10543 dense cortex with lucent center RGO:10545 ring epiphyses RGO:10545 DOID:12559 RGO:10550 juvenile osteoporosis RGO:10550 ivory epiphyses of hands and feet RGO:10552 dense epiphyses of hands and feet RGO:10552 SNOMEDCT:270505009 RGO:10565 Kashin-Beck disease RGO:10565 generalized physeal widening RGO:10569 generalized wide epiphyseal plate RGO:10569 localized physeal widening RGO:10581 localized wide epiphyseal plate RGO:10581 RGO:10587 Kirner deformity RGO:10587 RGO:10591 spondylometaphyseal dysplasias RGO:10591 RGO:10592 shortened bone with premature growth-plate closure RGO:10592 RGO:10598 neoplasm invading growth plate RGO:10598 RGO:10600 disrupted epiphyseal-metaphyseal junction RGO:10600 RGO:10603 fracture in weakened bone RGO:10603 RGO:10605 bone sarcoma RGO:10605 DOID:2491 HP:0000763 SNOMEDCT:95662005 RGO:10606 sensory neuropathy RGO:10606 SEMD Strudwick type Strudwick syndrome spondyloepiphyseal dysplasia congenita with dappled metaphyses ORDO:93346 RGO:10607 spondyloepimetaphyseal dysplasia Strudwick type RGO:10607 RGO:10608 radiolucent metaphyseal bands RGO:10608 RGO:10617 intrauterine gut perforation with meconium peritonitis RGO:10617 RGO:10619 transverse dense metaphyseal bands RGO:10619 RGO:10626 biphosphonate therapy RGO:10626 DOID:0060645 HP:0005901 ORDO:324964 RADLEX:RID3515 RGO:10627 chronic recurrent multifocal osteomyelitis RGO:10627 psychosocial dwarfism with trauma RGO:10629 deprivation dwarfism with trauma RGO:10629 HP:0005871 SNOMEDCT:28681006 RGO:10634 metaphyseal chondrodysplasia RGO:10634 RGO:10635 parathormone therapy RGO:10635 SNOMEDCT:57662003 RGO:10639 vascular injury RGO:10639 RGO:10640 dense vertical metaphyseal lines RGO:10640 SNOMEDCT:389207000 RGO:10644 mixed sclerosing bone dysplasia RGO:10644 RGO:10651 immunologic disorder RGO:10651 SNOMEDCT:238889004 RGO:10658 membranous lipodystrophy RGO:10658 short long bones with pronounced metaphyseal flaring RGO:10664 dumbbell bones RGO:10664 cup-shaped metaphyses HP:0003021 RGO:10666 metaphyseal cupping RGO:10666 RGO:10685 vitamin K deficiency embryopathy RGO:10685 DOID:5810 SNOMEDCT:44940001 RGO:10692 adenosine deaminase deficiency RGO:10692 RGO:10693 deferoxamine-induced bone dysplasia RGO:10693 RGO:10696 neurologic disorder with bone atrophy RGO:10696 RGO:10700 indistinct frayed metaphyses RGO:10700 RGO:10705 medial proximal metaphyseal erosion of the long bones RGO:10705 DOID:2601 RADLEX:RID4132 SNOMEDCT:9266000 RGO:10709 juxtacortical chondroma RGO:10709 HP:0003106 RGO:10712 subperiosteal bone resorption RGO:10712 RGO:10716 pseudohypohyperparathyroidism RGO:10716 SNOMEDCT:395183000 RGO:10717 subperiosteal hematoma RGO:10717 RGO:10718 subperiosteal osteomyelitis RGO:10718 SNOMEDCT:281387004 RGO:10742 regional osteoporosis RGO:10742 RGO:10756 congenital pseudarthrosis RGO:10756 HP:0040160 RGO:10762 generalized osteoporosis RGO:10762 DOID:13577 HP:0100510 SNOMEDCT:76169001 RGO:10766 vitamin C deficiency RGO:10766 DOID:319 HP:0002143 SNOMEDCT:48522003 RGO:10771 spinal cord disease RGO:10771 RGO:10772 space flight osteoporosis RGO:10772 RGO:10787 senile or postmenopausal osteoporosis RGO:10787 RGO:10789 histiocytic medullary reticulocytosis RGO:10789 HADD ICD10CM:M11.0 SNOMEDCT:239828000 RGO:10790 hydroxyapatite deposition disease RGO:10790 RGO:10797 congenital generalized osteoporosis RGO:10797 DOID:0050444 ICD10CM:G60.1 ORDO:772 SNOMEDCT:238062008 RGO:10802 infantile Refsum disease RGO:10802 DOID:0060849 ORDO:2788 RGO:10806 osteoporosis-pseudoglioma syndrome RGO:10806 RGO:10808 Thevenard syndrome RGO:10808 familial xanthomatosis DOID:14497 ORDO:75233 SNOMEDCT:82500001 RGO:10810 Wolman disease RGO:10810 HP:0002024 RGO:10812 malabsorption states RGO:10812 RGO:10814 mesenteric disease RGO:10814 RGO:10820 acquired chronic biliary obstruction RGO:10820 RGO:10822 renal osteomalacia RGO:10822 de Toni-Debré-Fanconi syndrome DOID:1062 SNOMEDCT:40488004 RGO:10824 Fanconi syndrome RGO:10824 RGO:10827 chronic obstructive renal disease RGO:10827 ICD10CM:E83.59 ORDO:2197 RGO:10828 idiopathic hypercalciuria RGO:10828 RTA DOID:14219 HP:0001947 SNOMEDCT:1776003 RGO:10830 renal tubular acidosis RGO:10830 RADLEX:RID1784 SNOMEDCT:57655007 RGO:10831 ureterosigmoidostomy RGO:10831 RGO:10834 congenital rickets RGO:10834 DOID:13381 SNOMEDCT:84027009 RGO:10841 pernicious anemia RGO:10841 RGO:10845 maternal magnesium sulfate therapy RGO:10845 SNOMEDCT:392559009 RGO:10848 tumor-induced osteomalacia RGO:10848 MPNST malignant schwannoma neurofibrosarcoma neurosarcoma DOID:5940 HP:0100697 ORDO:3148 RADLEX:RID4444 SNOMEDCT:19897006 SNOMEDCT:404037002 RGO:10853 malignant peripheral nerve sheath tumor RGO:10853 RGO:10859 reticuloses RGO:10859 RGO:10860 secretion of parathormone-like substance from malignant neoplasm RGO:10860 RGO:10864 glomerular failure RGO:10864 HP:0001941 ICD10CM:E87.2 SNOMEDCT:51387008 RGO:10865 acidosis RGO:10865 RGO:10866 malabsorption with reduced calcium absorption from intestine RGO:10866 RGO:10867 normal neonate RGO:10867 SNOMEDCT:70241007 RGO:10871 dietary deficiency RGO:10871 RGO:10873 increased carbohydrate metabolism RGO:10873 HP:0000124 RGO:10877 renal tubular dysfunction RGO:10877 RGO:10879 active reconstruction of bone RGO:10879 HP:0001948 ICD10CM:E87.3 SNOMEDCT:21420006 RGO:10880 alkalosis RGO:10880 HP:0012213 RGO:10881 decreased glomerular filtration rate RGO:10881 RGO:10882 widespread demineralization with coarse trabeculation RGO:10882 RGO:10887 idiopathic axial osteomalacia RGO:10887 RGO:10888 recalcification after disuse osteoporosis RGO:10888 RGO:10889 scattered decreased and increased bone density RGO:10889 AVN aseptic necrosis bone infarction ischemic bone necrosis osteonecrosis HP:0010885 RADLEX:RID34605 SNOMEDCT:86217007 RGO:10892 avascular necrosis RGO:10892 decompression sickness dysbaric osteonecrosis SNOMEDCT:89684003 RGO:10899 caisson disease RGO:10899 RGO:10909 spontaneous osteonecrosis of the knee RGO:10909 Blount osteonecrosis RGO:10915 osteonecrosis of the medial tibial condyle RGO:10915 RGO:10925 osteonecrosis of calcaneal apophysis RGO:10925 RGO:10926 osteonecrosis of capitulum of humerus RGO:10926 osteonecrosis of carpal scaphoid RADLEX:RID29079 RGO:10927 Preiser disease RGO:10927 Arkin disease Liffert disease RGO:10928 osteonecrosis of the distal tibial epiphysis RGO:10928 Caffey wrist osteonecrosis RGO:10930 osteonecrosis of entire carpus RGO:10930 diametaphyeal ischemia RGO:10943 bone infarct RGO:10943 RGO:10948 pancreatitis with fat necrosis RGO:10948 RGO:10950 bone-within-a-bone appearance RGO:10950 RGO:10954 bone diseases with a split or double layer cortex RGO:10954 SNOMEDCT:85866007 RGO:10956 heavy metal poisoning RGO:10956 RGO:10957 prostaglandin E1 therapy RGO:10957 SNOMEDCT:407523005 RGO:10961 bone sequestrum RGO:10961 RGO:10963 button sequestrum in skull RGO:10963 RADLEX:RID34622 RGO:10967 tropical ulcer RGO:10967 RGO:10968 multiple sclerotic foci in an infant or child RGO:10968 RGO:10984 solitary osteosclerotic bone lesion RGO:10984 RGO:10992 osteoblastic metastasis RGO:10992 DOID:84 HP:0010886 ICD10CM:M93.2 RADLEX:RID5381 SNOMEDCT:82562007 RGO:10993 osteochondritis dissecans RGO:10993 RGO:10996 condensing osteitis of clavicle RGO:10996 DOID:180 HP:0030426 RADLEX:RID4008 SNOMEDCT:25603007 RGO:11000 ossifying fibroma RGO:11000 RADLEX:RID3859 SNOMEDCT:21971004 RGO:11002 plasma cell granuloma RGO:11002 SAPHO syndrome synovitis - acne - pustulosis - hyperostosis - osteomyelitis syndrome RGO:11003 sternocostoclavicular hyperostosis RGO:11003 RGO:11005 multiple osteosclerotic bone lesions RGO:11005 RGO:11016 osteosarcomatosis RGO:11016 RGO:11018 widespread osteosclerosis RGO:11018 RGO:11024 congenital cyanotic heart disease RGO:11024 HO HOA RADLEX:RID34789 SNOMEDCT:203357004 RGO:11029 hypertrophic osteoarthropathy RGO:11029 RGO:11032 idiopathic familial osteosclerosis RGO:11032 RGO:11037 congenital widespread osteosclerosis RGO:11037 RGO:11038 physiologic osteosclerosis of newborn RGO:11038 RGO:11045 osteoblastic metastases RGO:11045 RGO:11047 sickle cell disease and variants RGO:11047 RGO:11053 osteosclerosis with dentine dysplasia RGO:11053 Codman tumor DOID:2649 HP:0030432 RADLEX:RID4134 SNOMEDCT:9001003 RGO:11055 chondroblastoma RGO:11055 DOID:5867 RADLEX:RID4142 SNOMEDCT:128775007 RGO:11056 clear cell chondrosarcoma RGO:11056 RGO:11058 intraosseous ganglion RGO:11058 RGO:11061 metaphyseal bone lesion RGO:11061 RADLEX:RID4135 SNOMEDCT:39553005 RGO:11063 chondromyxoid fibroma RGO:11063 RGO:11064 cortical/periosteal desmoid RGO:11064 RGO:11071 parosteal sarcoma RGO:11071 RGO:11073 diametaphyseal bone lesion RGO:11073 RGO:11077 diaphyseal bone lesion RGO:11077 RGO:11094 solitary well-defined lytic metaphyseal lesion RGO:11094 DOID:2776 ORDO:55881 RADLEX:RID4179 SNOMEDCT:20462008 RGO:11095 adamantinoma RGO:11095 RGO:11103 solitary ill-defined lytic metaphyseal lesion RGO:11103 RGO:11111 solitary permeative metaphyseal lesion RGO:11111 RGO:11115 solitary lytic diaphyseal bone lesion RGO:11115 RGO:11126 lucent bone lesion with sclerotic rim RGO:11126 bone abscess RADLEX:RID3513 SNOMEDCT:63375009 RGO:11127 Brodie abscess RGO:11127 LSMFT RGO:11134 liposclerosing myxofibrous tumor RGO:11134 RGO:11136 solitary well-demarcated lytic bone lesion RGO:11136 SNOMEDCT:3875003 SNOMEDCT:402469004 RGO:11138 gouty tophus RGO:11138 RADLEX:RID4024 SNOMEDCT:78453009 RGO:11149 telangiectatic osteosarcoma RGO:11149 DOID:2601 RADLEX:RID4132 SNOMEDCT:9266000 RGO:11150 periosteal chondroma RGO:11150 SNOMEDCT:53305005 RGO:11151 periosteal fibroma RGO:11151 RGO:11152 well-defined infectious bone lesion RGO:11152 RGO:11159 solitary bone lesion with expansile remodeling RGO:11159 SNOMEDCT:203470009 RGO:11168 fibrous cortical defect RGO:11168 solitary eccentric bone lesion with expansile remodeling RGO:11171 bone blister RGO:11171 solitary bone lesion with marked expansile remodeling RGO:11178 blow-out bone lesion RGO:11178 RGO:11185 large destructive bone lesion RGO:11185 RGO:11192 solitary poorly demarcated osteolytic bone lesion RGO:11192 moth-eaten osteolytic lesion RGO:11195 permeative osteolytic lesion RGO:11195 multifocal granulomatous osteomyelitis in a compromised child RGO:11199 Landing-Shirkey disease RGO:11199 RGO:11201 osteolytic lesion with calcium attenuation RGO:11201 RGO:11210 bone lesion with fluid-fluid level RGO:11210 RGO:11215 multiple radiolucent bone lesions RGO:11215 DOID:9120 HP:0011034 ICD10CM:E85 RADLEX:RID5188 SNOMEDCT:17602002 RGO:11218 amyloidosis RGO:11218 RGO:11220 electrical injury RGO:11220 driller disease of wrists vibration syndrome RGO:11224 jackhammer operator disease RGO:11224 RGO:11228 polyvinyl chloride osteolysis RGO:11228 RGO:11230 radium poisoning RGO:11230 RGO:11232 silastic arthropathy RGO:11232 RGO:11234 widespread areas of bone destruction RGO:11234 RGO:11244 hemophilia with pseudotumors RGO:11244 Hansen disease DOID:1024 ORDO:548 SNOMEDCT:81004002 RGO:11245 leprosy RGO:11245 HP:0002797 ICD10CM:M89.5 RADLEX:RID5382 SNOMEDCT:203522001 SNOMEDCT:30425001 RGO:11246 osteolysis RGO:11246 bankokerend dactylolysis spontanea sukhapakla DOID:11329 HP:0031009 ICD10CM:L94.6 SNOMEDCT:38528001 RGO:11250 ainhum RGO:11250 RGO:11254 osteolysis with detritic synovitis RGO:11254 RGO:11255 rapidly progressive coxarthrosis RGO:11255 SNOMEDCT:8664001 RGO:11270 fibromyxoma RGO:11270 RADLEX:RID3989 SNOMEDCT:33176006 SNOMEDCT:403977003 RGO:11276 malignant hemangioendothelioma RGO:11276 RGO:11284 benign bone neoplasm RGO:11284 RGO:11289 non-neoplastic bone lesion RGO:11289 RGO:11301 xanthomatous lesion RGO:11301 RGO:11302 benign fibrocystic bone lesion RGO:11302 ORDO:57782 SNOMEDCT:699251001 RGO:11311 Mazabraud syndrome RGO:11311 RGO:11313 xanthomatous bone lesion RGO:11313 DOID:4810 ORDO:909 RADLEX:RID5130 SNOMEDCT:63246000 RGO:11317 cerebrotendinous xanthomatosis RGO:11317 RGO:11322 primary aneurysmal bone cyst RGO:11322 RGO:11326 malignant primary bone neoplasm RGO:11326 RADLEX:RID35093 RGO:11338 Codman triangle RGO:11338 DOID:3347 HP:0002669 ORDO:668 RADLEX:RID4010 SNOMEDCT:21708004 SNOMEDCT:307576001 RGO:11344 osteosarcoma RGO:11344 SNOMEDCT:404077005 RGO:11346 extraskeletal osteosarcoma RGO:11346 fibrogenic osteosarcoma RADLEX:RID4013 SNOMEDCT:12690005 RGO:11347 fibroblastic osteosarcoma RGO:11347 osteoclast-rich osteosarcoma RGO:11348 giant cell-rich osteosarcoma RGO:11348 mandibular osteosarcoma RADLEX:RID4014 SNOMEDCT:431911000124102 RGO:11349 gnathic osteosarcoma RGO:11349 RGO:11350 high-grade surface osteosarcoma RGO:11350 RADLEX:RID4016 SNOMEDCT:128774006 RGO:11351 intracortical osteosarcoma RGO:11351 central osteosarcoma classical osteosarcoma conventional osteosarcoma high-grade osteolytic osteosarcoma RGO:11352 high-grade intramedullary osteosarcoma RGO:11352 sclerosing osteosarcoma RGO:11353 low-grade intramedullary osteosarcoma RGO:11353 RGO:11363 metallic implant RGO:11363 DOID:3371 HP:0006765 ORDO:55880 RADLEX:RID4140 SNOMEDCT:14990007 SNOMEDCT:443520009 RGO:11366 chondrosarcoma RGO:11366 RGO:11370 juxtacortical or periosteal RGO:11370 RGO:11377 round cell bone lesion RGO:11377 RGO:11384 tumor-like bone destruction with little periosteal reaction RGO:11384 RGO:11387 bone tumor with periosteal reaction RGO:11387 RGO:11400 meningiosarcoma RGO:11400 lytic bone metastasis lytic skeletal metastasis RGO:11403 osteolytic metastasis RGO:11403 RGO:11409 carcinoma of cervix or uterus RGO:11409 RGO:11423 tumor-like bone surface lesion RGO:11423 acquired osteochondroma RADLEX:RID35668 RGO:11428 turret exostosis RGO:11428 BPOP RGO:11430 bizarre parosteal pseudotumor RGO:11430 RADLEX:RID4354 SNOMEDCT:473437005 RGO:11436 parosteal lipoma RGO:11436 DOID:1019 HP:0002754 ICD10CM:M86 RADLEX:RID3715 SNOMEDCT:60168000 RGO:11443 osteomyelitis RGO:11443 RADLEX:RID35253 RGO:11445 spiculated periosteal reaction RGO:11445 RADLEX:RID5420 SNOMEDCT:237826006 RGO:11452 thyroid acropachy RGO:11452 RGO:11453 localized periosteal reaction RGO:11453 SNOMEDCT:264516005 RGO:11455 dactylitis RGO:11455 RGO:11463 benign bone cyst or neoplasm with expansion or pathologic fracture RGO:11463 generalized periosteal reaction RGO:11470 widespread periosteal reaction RGO:11470 RGO:11478 Cushing syndrome with excess callus RGO:11478 RGO:11479 florid reactive periostitis of the phalanges RGO:11479 RGO:11491 periosteal new bone formation in a child RGO:11491 child abuse RGO:11503 battered child syndrome RGO:11503 RGO:11507 scapular fractures RGO:11507 RGO:11508 spinous process fracture RGO:11508 SNOMEDCT:78516000 RGO:11509 sternal fracture RGO:11509 RGO:11512 bilateral fractures RGO:11512 RGO:11513 fractures at different stages of healing RGO:11513 RGO:11514 epiphyseal separations RGO:11514 RGO:11515 vertebral subluxations RGO:11515 RGO:11516 fractures of digits of hands or feet RGO:11516 RGO:11517 complex skull fracture RGO:11517 RGO:11519 subperiosteal new bone formation RGO:11519 RGO:11521 clavicular fracture RGO:11521 RGO:11522 fractures of shafts of long bones RGO:11522 RGO:11523 simple linear skull fractures RGO:11523 RGO:11527 intramural intestinal hematoma RGO:11527 RGO:11528 solid organ laceration RGO:11528 RGO:11531 excess callus formation RGO:11531 RGO:11534 paralytic disorders RGO:11534 RGO:11536 sclerosis of bone with periosteal reaction RGO:11536 RGO:11537 healing fracture with callus RGO:11537 RGO:11543 arteriovenous fistula of lung RGO:11543 RGO:11545 chronic gastrointestinal disease RGO:11545 DOID:6760 RGO:11550 lymphoma of lung RGO:11550 RGO:11555 thick periosteal reaction along bone shaft RGO:11555 RGO:11566 tropical ulcer osteoma RGO:11566 RGO:11568 localized cortical bone thickening RGO:11568 RGO:11577 widespread cortical bone thickening RGO:11577 RGO:11581 hyperostosis generalisata with striation of bones RGO:11581 RGO:11582 prostaglandin-induced hyperostosis RGO:11582 RGO:11583 widespread cortical bone thinning RGO:11583 double-layer cortex RGO:11588 split cortex RGO:11588 RGO:11593 removed intramedullary rod RGO:11593 erosion of the inner cortical margin resorption of the inner cortical margin scalloping of the inner cortical margin RGO:11595 loss of inner cortical bone margin RGO:11595 RGO:11598 erosion of cortical bone surface RGO:11598 RGO:11604 primary bone neoplasm RGO:11604 proliferation of new bone at tendon and ligament insertion RGO:11614 bony whiskering RGO:11614 DOID:8553 HP:0025452 ICD10CM:L88 ORDO:48104 SNOMEDCT:74578003 RGO:11617 pyoderma gangrenosum RGO:11617 RGO:11618 syphilis of spine RGO:11618 RGO:11620 polyostotic bone lesions in adults RGO:11620 RGO:11621 arthritic or synovial-based lesions RGO:11621 RGO:11631 polyostotic bone lesions in children RGO:11631 RGO:11633 osteochondrodysplasias and dysostoses RGO:11633 RGO:11640 polyostotic bone lesions in an infant or young child RGO:11640 DOID:11338 ORDO:3299 SNOMEDCT:76902006 RGO:11645 tetanus RGO:11645 RGO:11648 juvenile idiopathic osteoporosis RGO:11648 RGO:11649 spondylometaphyseal dysplasia corner fracture type RGO:11649 DOID:13366 ICD10CM:G25.82 ORDO:3198 SNOMEDCT:5217008 RGO:11650 stiff-man syndrome RGO:11650 HP:0002757 SNOMEDCT:134291007 RGO:11653 multiple fractures RGO:11653 RGO:11660 aluminum-induced bone disease RGO:11660 RGO:11682 pseudofracture RGO:11682 ICD10CM:M84.3 RADLEX:RID4695 SNOMEDCT:23382007 SNOMEDCT:240197007 RGO:11685 stress fracture RGO:11685 RGO:11688 radiation osteitis RGO:11688 HP:0005864 SNOMEDCT:31511007 SNOMEDCT:410818009 RGO:11722 pseudoarthrosis RGO:11722 pencil-pointing of bone RGO:11733 vascular deossification RGO:11733 pyarthrosis DOID:813 HP:0003095 RADLEX:RID3614 SNOMEDCT:48245008 RGO:11735 septic arthritis RGO:11735 Trevor disease ORDO:1822 SNOMEDCT:205480005 RGO:11749 dysplasia epiphysealis hemimelica RGO:11749 osteo-onychodysplasia DOID:9467 ORDO:2614 SNOMEDCT:22199006 RGO:11751 nail-patella syndrome RGO:11751 RGO:11752 pelvic digit or rib RGO:11752 SNOMEDCT:26904005 SNOMEDCT:703697003 RGO:11755 subungual exostosis RGO:11755 RGO:11756 supracondylar spur of humerus RGO:11756 RGO:11759 synostosis of tubular bones RGO:11759 RGO:11762 humeroradial-humeroulnar synostosis RGO:11762 DOID:9827 HP:0002974 ICD10CM:Q74.0 SNOMEDCT:33313004 RGO:11766 radioulnar synostosis RGO:11766 RGO:11768 gas within bone RGO:11768 RGO:11769 methylmethacrylate prosthesis RGO:11769 HP:0009777 RGO:11774 absent thumb RGO:11774 ICD10CM:Q75.4 RGO:11775 Franceschetti syndrome RGO:11775 HP:0009778 SNOMEDCT:253936008 RGO:11777 hypoplastic thumb RGO:11777 ICD10CM:Q87.0 SNOMEDCT:205260006 RGO:11778 acrocephalopolysyndactyly RGO:11778 ORDO:2307 RGO:11782 IVIC syndrome RGO:11782 WL syndrome symphalangism-brachydactyly syndrome RGO:11786 symphalangism-surdity syndrome RGO:11786 chromosome 9:dup(9p) syndrome ORDO:236 RGO:11787 trisomy 9p RGO:11787 RGO:11788 wide thumb RGO:11788 RGO:11789 frontodigital syndrome RGO:11789 RGO:11790 enlarged thumb RGO:11790 abnormal position of thumb RGO:11794 ectopic thumb RGO:11794 DR syndrome Okihiro syndrome DOID:0060747 SNOMEDCT:699867001 RGO:11800 Duane-radial ray syndrome RGO:11800 ORDO:65798 RGO:11801 Goodman syndrome RGO:11801 RGO:11804 short broad distal phalanx of thumb RGO:11804 RGO:11806 short thin distal phalanx of thumb RGO:11806 RGO:11807 short proximal phalanx RGO:11807 RGO:11811 drumstick distal phalanges RGO:11811 RGO:11812 broad distal phalanx of thumb RGO:11812 RGO:11814 mesomelic dysplasia Robinow type RGO:11814 HP:0009836 RGO:11816 broad distal phalanges RGO:11816 RGO:11818 distal brachydactyly RGO:11818 RGO:11820 broad middle phalanges RGO:11820 RGO:11824 familial brachydactyly A1 RGO:11824 RGO:11826 congenital abnormality of great toe RGO:11826 duplicated great toe duplicated hallux duplication of hallux hallucal polydactyly RGO:11828 duplication of great toe RGO:11828 incurving of fifth digit with hypoplastic short middle phalanx RGO:11829 clinodactyly of fifth finger RGO:11829 HP:0005819 RGO:11841 short middle phalanges RGO:11841 RGO:11845 short and broad distal phalanges of hand RGO:11845 RGO:11847 thin and small distal phalanges of the hand RGO:11847 RGO:11848 hypoplastic nails syndrome RGO:11848 spindle-shaped terminal phalanges stubby terminal phalanges HP:0009882 RGO:11849 hypoplastic terminal phalanges RGO:11849 RGO:11852 spade hand RGO:11852 RGO:11853 familial brachydactyly B RGO:11853 DOID:5160 SNOMEDCT:361133006 RGO:11855 arteriosclerosis obliterans RGO:11855 SNOMEDCT:25907005 RGO:11856 diabetic gangrene RGO:11856 Raynaud syndrome DOID:10300 HP:0030880 SNOMEDCT:195295006 RGO:11859 Raynaud disease RGO:11859 thromboangiitis obliterans ORDO:36258 RADLEX:RID3310 RGO:11863 Buerger disease RGO:11863 HP:0100759 ICD10CM:R68.3 RGO:11864 clubbing of fingers RGO:11864 RGO:11866 hunger osteopathy RGO:11866 ORDO:2897 RGO:11868 pityriasis rubra RGO:11868 RGO:11869 plantar warts RGO:11869 RGO:11872 acquired acro-osteolysis of one digit RGO:11872 RGO:11873 carcinoma of nail bed RGO:11873 DOID:314 SNOMEDCT:128777004 SNOMEDCT:95413004 RGO:11874 giant cell tumor of tendon sheath RGO:11874 RGO:11876 band-like erosion of the midportion of a terminal phalanx RGO:11876 terminal phalangeal sclerosis RGO:11880 acro-osteosclerosis RGO:11880 RGO:11882 acquired absence of phalanx, digit, hand, or foot RGO:11882 RGO:11884 surgical amputation RGO:11884 RGO:11893 congenital absence of phalanx, digit, hand, or foot RGO:11893 HP:0001171 RADLEX:RID35084 SNOMEDCT:299034005 RGO:11896 claw hand RGO:11896 HP:0000742 SNOMEDCT:130968006 RGO:11899 self-mutilation RGO:11899 RGO:11901 gangrene of finger or toe RGO:11901 ICD10CM:T69.02 SNOMEDCT:234015005 RGO:11912 trench foot RGO:11912 RGO:11913 trophic ulcer with underlying destruction RGO:11913 RGO:11914 lytic phalangeal lesion RGO:11914 ICD10CM:M67.4 RADLEX:RID13191 SNOMEDCT:71307009 RGO:11920 ganglion RGO:11920 RGO:11925 thorn granuloma RGO:11925 HP:0001114 RADLEX:RID5221 SNOMEDCT:63103006 SNOMEDCT:75594004 RGO:11926 xanthoma RGO:11926 M. tuberculosis TB DOID:399 ORDO:3389 RADLEX:RID29116 SNOMEDCT:56717001 RGO:11929 tuberculosis RGO:11929 ORDO:352636 RGO:11934 phalangeal microgeodic syndrome RGO:11934 RGO:11936 clubbing of digits RGO:11936 DOID:5157 ICD10CM:C45.0 RGO:11942 mesothelioma of pleura RGO:11942 fusion of phalanges in a digit DOID:11193 RGO:11945 symphalangism RGO:11945 RGO:11949 Cushing symphalangism RGO:11949 RGO:11951 contracture of a digit RGO:11951 congenital contractural arachnofactyly ORDO:115 SNOMEDCT:205821003 RGO:11954 congenital contractural arachnodactyly RGO:11954 HP:0005679 SNOMEDCT:274142002 RGO:11956 Dupuytren contracture RGO:11956 RGO:11958 Volkmann ischemic contracture RGO:11958 CAP syndrome PAC syndrome camptodactyly-arthropathy syndrome camptodactyly-arthropathy-pericarditis syndrome pericarditis-arthropathy-camptodactyly syndrome DOID:0090127 RGO:11966 arthropathy-camptodactyly syndrome RGO:11966 ORDO:1319 RGO:11967 camptobrachydactyly RGO:11967 RGO:11968 camptodactyly-ankylosis-pulmonary hypoplasia syndrome RGO:11968 ORDO:574 RGO:11970 monosomy 21 syndrome RGO:11970 ORDO:3292 RGO:11971 Tel Hashomer camptodactyly syndrome RGO:11971 soft tissue union, with or without osseous union, between adjacent digits DOID:11193 HP:0001159 ICD10CM:Q70 SNOMEDCT:373413006 RGO:11972 syndactyly RGO:11972 RGO:11978 acro-pectoro-vertebral dysplasia RGO:11978 ORDO:1396 RGO:11979 cerebro-renal-digital syndrome RGO:11979 DOID:0050887 ORDO:857 RGO:11982 Townes-Brocks syndrome RGO:11982 ulnar-side polydactyly DOID:1148 HP:0100259 RGO:11983 postaxial polydactyly RGO:11983 McKusick-Kaufman syndrome hereditary hydrometrocolpos hydrometrocolpos - postaxial polydactyly ORDO:2473 RGO:11984 Kaufman-McKusick syndrome RGO:11984 holoprosencephaly-polydactyly syndrome SNOMEDCT:716091000 RGO:11985 pseudotrisomy 13 syndrome RGO:11985 HP:0004099 SNOMEDCT:48449000 RGO:11986 macrodactyly RGO:11986 SNOMEDCT:41252002 RGO:11990 plexiform neuroma RGO:11990 RGO:11993 ichthyosis syndrome RGO:11993 47,XYY syndrome chromosome XYY syndrome disomy Y double Y syndrome ORDO:8 SNOMEDCT:50749006 RGO:11995 XYY syndrome RGO:11995 RGO:11996 localized brachydactyly RGO:11996 RGO:12005 familial brachydactylies RGO:12005 RGO:12007 radiation or radium injury RGO:12007 congenital acromelia RGO:12008 congenital short hands and feet RGO:12008 chondrodysplasia punctata X-linked recessive brachytelephalangic type ORDO:79345 RGO:12011 chondrodysplasia punctata brachytelephalangic type RGO:12011 RGO:12012 familial brachdactyly syndromes RGO:12012 fibular aplasia - complex brachydactyly syndrome DOID:0050790 SNOMEDCT:715474004 RGO:12042 du Pan syndrome RGO:12042 RGO:12050 megaepiphyseal dwarfism RGO:12050 short 4th metacarpal RGO:12065 short fourth metacarpal RGO:12065 RGO:12067 sickle cell disease with infarction RGO:12067 RGO:12069 familial brachydactyly E RGO:12069 RGO:12070 acquired short hands and feet RGO:12070 ORDO:1146 SNOMEDCT:715314008 RGO:12076 digitotalar dysmorphism RGO:12076 RGO:12078 large hands for age RGO:12078 RGO:12082 asymmetrically small bones of one hand RGO:12082 RGO:12085 arrested epiphyseal growth RGO:12085 RGO:12086 asymmetrically large bones of one hand RGO:12086 osseous neoplasm DOID:184 HP:0010622 RGO:12087 bone neoplasm RGO:12087 RADLEX:RID4873 SNOMEDCT:30098003 RGO:12088 hyperemia RGO:12088 RGO:12090 generalized asymmetry of hand bones RGO:12090 HP:0100556 SNOMEDCT:34087007 RGO:12091 hemiatrophy RGO:12091 failure of bone tubulation in the hand generalized failure of bony modeling in the hand RGO:12093 thick tubular hand bones RGO:12093 RGO:12100 proximal tapering of short tubular bones of the hands and feet RGO:12100 RGO:12102 distal tapering of short tubular bones of the hands and feet RGO:12102 RGO:12104 neuropathic bone changes of the hands or feet RGO:12104 RGO:12110 trophic ulcer of soft tissue with underlying destruction RGO:12110 RGO:12112 amyloid neuropathy RGO:12112 RGO:12113 Charcot-Marie-Tooth syndrome RGO:12113 RGO:12114 ergot intoxication RGO:12114 SNOMEDCT:73590005 RGO:12117 peripheral nerve injury RGO:12117 RGO:12118 lucent defect in bones of hands, wrists, feet, or ankles RGO:12118 RGO:12136 vascular channel RGO:12136 DOID:9898 RADLEX:RID3648 RGO:12137 villonodular synovitis RGO:12137 RGO:12145 intraosseous gouty tophus calcification RGO:12145 RGO:12155 smallpox residual RGO:12155 RGO:12157 congenital foot deformity RGO:12157 RGO:12158 faulty intrauterine positioning RGO:12158 lucent calcaneal lesion RGO:12170 lucent lesion of the calcaneus RGO:12170 RGO:12178 accessory carpal or tarsal bones RGO:12178 RGO:12179 anatomic variant RGO:12179 RGO:12180 fragmented, irregular, or sclerotic carpal or tarsal bones RGO:12180 RGO:12186 congenital bipartite bone RGO:12186 RGO:12188 mixed sclerotic bone dysplasia RGO:12188 ORDO:93314 RGO:12193 spondylometaphyseal dysplasia Kozlowski type RGO:12193 RGO:12195 small or dysplastic carpal and/or tarsal bones RGO:12195 RGO:12199 carpal and/or tarsal fusion RGO:12199 HP:0100257 RGO:12205 cleft hand or foot RGO:12205 acropectorovertebral syndrome RGO:12208 F syndrome RGO:12208 familial tylosis keratosis palmaris et plantaris familiaris DOID:0050428 SNOMEDCT:26996000 SNOMEDCT:399955009 RGO:12210 tylosis RGO:12210 carpal angle less than 124 degrees RGO:12211 decreased carpal angle RGO:12211 carpal angle greater than 139 degrees RGO:12214 increased carpal angle RGO:12214 RGO:12215 Pfeiffer-like syndrome RGO:12215 hypoplasia or aplasia of radius and/or thumb and lateral carpal bones RGO:12217 radial ray syndrome RGO:12217 RGO:12218 facioauriculoradial dysplasia RGO:12218 ORDO:291 SNOMEDCT:715223009 RGO:12219 fetal varicella syndrome RGO:12219 hypoplasia or aplasia of the ulna and/or fourth and fifth fingers RGO:12221 ulnar ray syndrome RGO:12221 Miller syndrome RGO:12226 Miller postaxial acrofacial dysostosis syndrome RGO:12226 DOID:0060614 ORDO:3138 SNOMEDCT:700211007 RGO:12227 ulnar-mammary syndrome RGO:12227 RGO:12228 Weyers oligodactyly syndrome RGO:12228 deformity of forearm RGO:12233 forearm deformity RGO:12233 RGO:12237 proximal radioulnar dislocation RGO:12237 RGO:12238 congenital radioulnar synostosis RGO:12238 RGO:12247 congenital elbow anomaly RGO:12247 RGO:12249 radiohumeral synostosis RGO:12249 RGO:12251 displaced elbow fat pad RGO:12251 RGO:12253 trauma with hemorrhage RGO:12253 Reichel syndrome Reichel-Jones-Henderson syndrome SOC primary synovial osteochondromatosis synovial chondromatosis synovial chondrometaplasia RADLEX:RID35322 RADLEX:RID4139 SNOMEDCT:133850008 SNOMEDCT:202574006 RGO:12256 synovial osteochondromatosis RGO:12256 DOID:5485 HP:0012570 ORDO:3273 RADLEX:RID4558 SNOMEDCT:302851001 SNOMEDCT:63211008 RGO:12257 synovial sarcoma RGO:12257 RGO:12258 humeral head deformity RGO:12258 RGO:12264 Erb palsy with disuse RGO:12264 RGO:12265 glenohumeral dysplasia RGO:12265 RGO:12266 periarthrosis humeroscapularis RGO:12266 RGO:12267 rotator cuff tear with atrophy and upward subluxation RGO:12267 RGO:12269 congenitally abnormal scapula RGO:12269 RGO:12270 familial glenoid hypoplasia RGO:12270 PLSD Luton type RGO:12276 platyspondylic lethal skeletal dysplasia Luton type RGO:12276 RGO:12277 scapuloiliac dysostosis RGO:12277 RGO:12278 scapular lesion in an infant or child RGO:12278 SNOMEDCT:6836001 RGO:12283 brachial plexus injury RGO:12283 RGO:12285 clavicular lesion in an infant or child RGO:12285 RGO:12290 condensing osteitis of the clavicle RGO:12290 lateral clavicle hook RGO:12293 handlebar clavicle RGO:12293 RGO:12297 posttraumatic osteolysis RGO:12297 RGO:12301 premature infants RGO:12301 RGO:12303 congenital clavicular pseudoarthrosis RGO:12303 RGO:12308 elongated clavicle RGO:12308 broad clavicle enlarged clavicle RGO:12309 thick clavicle RGO:12309 RGO:12319 fracture with callus RGO:12319 DOID:14021 RGO:12323 Tietze syndrome RGO:12323 RGO:12324 distal clavicle defect RGO:12324 RGO:12331 neurogenic osteolysis RGO:12331 RGO:12333 tibiotalar tilt RGO:12333 HP:0002980 RGO:12339 femoral bowing RGO:12339 DOID:4953 ORDO:2912 SNOMEDCT:398102009 RGO:12341 poliomyelitis RGO:12341 RGO:12342 isolated tibial bowing RGO:12342 RGO:12350 elongation of fibula RGO:12350 RGO:12353 absence or hypoplasia of tibia RGO:12353 RGO:12364 normal-variant bipartite patella RGO:12364 acrocephalopolysyndactyly Carpenter type acrocephalopolysyndactyly type 2 DOID:0060234 ORDO:65759 SNOMEDCT:205813009 RGO:12366 Carpenter syndrome RGO:12366 RGO:12369 familial absence of the patella RGO:12369 RGO:12376 small patella syndrome RGO:12376 cerebrohepatorenal syndrome DOID:905 ICD10CM:E71.510 ORDO:912 SNOMEDCT:88469006 RGO:12381 Zellweger syndrome RGO:12381 high patella RADLEX:RID39259 RGO:12382 patella alta RGO:12382 RGO:12383 arthritis with joint effusion RGO:12383 DOID:13357 SNOMEDCT:36071006 RGO:12384 chondromalacia of patella RGO:12384 osteonecrosis of the tibial tubercle DOID:7489 ORDO:97335 RADLEX:RID5377 RGO:12386 Osgood-Schlatter disease RGO:12386 SNOMEDCT:1551001 RGO:12387 osteomyelitis of femur RGO:12387 SNOMEDCT:30832001 RGO:12388 rupture of patellar tendon RGO:12388 low patella patella profunda RADLEX:RID39260 RGO:12391 patella baja RGO:12391 SNOMEDCT:6849006 RGO:12394 rupture of quadriceps tendon RGO:12394 RGO:12395 surgical transposition of tibial tuberosity RGO:12395 RGO:12396 lytic patellar lesion RGO:12396 RGO:12397 dorsal defect of patella RGO:12397 RGO:12400 enlarged distal femoral intercondylar notch RGO:12400 ICD10CM:A18.01 RADLEX:RID34699 SNOMEDCT:190710003 RGO:12402 tuberculous arthritis RGO:12402 RGO:12403 enlarged medial femoral condyle RGO:12403 ICD10CM:E83.31 SNOMEDCT:82236004 RGO:12404 vitamin D-resistant rickets RGO:12404 RGO:12406 femoral anteversion RGO:12406 RGO:12410 physiologic tibial torsion in infants RGO:12410 SNOMEDCT:1360005 RGO:12418 physiologic RGO:12418 HP:0002812 RGO:12427 coxa vara RGO:12427 RGO:12433 idiopathic coxa vara RGO:12433 JRA DOID:676 HP:0005681 RADLEX:RID3610 SNOMEDCT:410795001 RGO:12437 juvenile rheumatoid arthritis RGO:12437 ICD10CM:Q65.82 SNOMEDCT:74820003 RGO:12438 congenital coxa vara RGO:12438 HP:0002673 SNOMEDCT:299236004 RGO:12441 coxa valga RGO:12441 RGO:12442 chronic leg injury RGO:12442 DDH congenital hip dysplasia developmental hip dysplasia DOID:9353 SNOMEDCT:52781008 RGO:12444 developmental dysplasia of the hip RGO:12444 SNOMEDCT:389160009 RGO:12447 spondyloepiphyseal dysplasia with joint laxity RGO:12447 RGO:12448 abnormal proximal femur RGO:12448 RGO:12454 femoral head dysplasia RGO:12454 ORDO:2623 SNOMEDCT:28557005 RGO:12459 geleophysic dysplasia RGO:12459 RGO:12460 fragmented or irregular femoral head RGO:12460 ORDO:2499 SNOMEDCT:205481009 RGO:12467 metachondromatosis RGO:12467 HP:0003179 ICD10CM:M24.7 SNOMEDCT:59606006 RGO:12478 protrusio acetabuli RGO:12478 RGO:12489 congenitally abnormal pelvis RGO:12489 DOID:4480 ICD10CM:Q77.4 ORDO:15 RADLEX:RID34620 SNOMEDCT:86268005 RGO:12490 achondroplasia RGO:12490 Jeune syndrome RGO:12494 asphyxiating thoracic dysplasia RGO:12494 DOID:0050463 ORDO:140 RGO:12495 campomelic dysplasia RGO:12495 MOPD1 Majewski osteodysplastic primordial dwarfism type 1 Taybi-Linder cephaloskeletal dysplasia Taybi-Linder syndrome microcephalic osteodysplastic primordial dwarfism type 1 osteodysplastic primordial dwarfism type 1 DOID:0060608 RGO:12497 cephaloskeletal dysplasia RGO:12497 DOID:2581 ICD10CM:Q77.3 SNOMEDCT:278715001 RGO:12498 chondrodysplasia punctata RGO:12498 SNOMEDCT:82699004 RGO:12504 Dyggve-Melchior-Clausen dysplasia RGO:12504 RGO:12505 dyssegmental dysplasia RGO:12505 DOID:0060465 ORDO:2021 SNOMEDCT:17144009 RGO:12506 fibrochondrogenesis RGO:12506 DOID:0080044 ICD10CM:Q77.0 ORDO:93297 SNOMEDCT:205483007 RGO:12508 hypochondrogenesis RGO:12508 DOID:0080041 ICD10CM:Q77.4 ORDO:429 SNOMEDCT:205468002 RGO:12509 hypochondroplasia RGO:12509 DOID:0080045 ORDO:485 SNOMEDCT:53974002 RGO:12510 Kniest dysplasia RGO:12510 DOID:14323 ORDO:558 SNOMEDCT:19346006 RGO:12511 Marfan syndrome RGO:12511 Shwachman-Bodian-Diamond syndrome metaphyseal chondrodysplasia Shwachman type RGO:12512 Shwachman–Diamond syndrome RGO:12512 ORDO:2635 SNOMEDCT:22764001 RGO:12513 metatropic dysplasia RGO:12513 Melnick-Needles dysplasia Melnick-Needles syndrome osteodysplasty osteodysplasty Melnick-Needles type ORDO:2484 RGO:12514 Melnick-Needles osteodysplasty RGO:12514 parastremmatic dwarfism RGO:12517 parastremmatic dysplasia RGO:12517 DOID:1933 ICD10CM:Q87.2 ORDO:783 SNOMEDCT:45582004 RGO:12518 Rubinstein-Taybi syndrome RGO:12518 spondyloepiphyseal dysplasia congenital DOID:0080025 DOID:14789 ORDO:94068 SNOMEDCT:278713008 RGO:12521 spondyloepiphyseal dysplasia congenita RGO:12521 thanatophoric dwarfism DOID:13481 ORDO:2655 RADLEX:RID46049 SNOMEDCT:29352008 RGO:12523 thanatophoric dysplasia RGO:12523 RGO:12531 serrated iliac crests RGO:12531 RGO:12532 narrow pelvis in an infant or child RGO:12532 RGO:12535 pelvic exostosis RGO:12535 triradiate acetabulum RGO:12538 trident pelvis RGO:12538 RGO:12539 type A pelvis RGO:12539 RGO:12542 chondrodysplasia punctata rhizomelic type RGO:12542 RGO:12544 type B pelvis RGO:12544 RGO:12545 acrocephalosyndactyly Waardenburg type RGO:12545 SNOMEDCT:205425003 RGO:12550 sacral agenesis RGO:12550 RGO:12551 defective pubic ossification RGO:12551 RGO:12553 familial pubic diastasis RGO:12553 thanatophoric variant RGO:12555 thanatophoric dysplasia variant RGO:12555 pubic diastasis HP:0003183 RGO:12556 wide pubic symphysis RGO:12556 SNOMEDCT:125673005 RGO:12558 traumatic dislocation RGO:12558 HP:0001540 SNOMEDCT:62629000 RGO:12562 diastasis recti RGO:12562 RGO:12568 bridging of the pubic symphysis RGO:12568 DOID:668 SNOMEDCT:44551007 RGO:12574 myositis ossificans RGO:12574 RGO:12576 eleven pairs of ribs RGO:12576 RGO:12577 thirteen pairs of ribs RGO:12577 RGO:12583 regenerated rib after resection RGO:12583 SNOMEDCT:14350002 SNOMEDCT:205562004 RGO:12584 angiomatosis RGO:12584 spondylothoracic dysostosis DOID:0050568 SNOMEDCT:61367005 RGO:12587 spondylothoracic dysplasia RGO:12587 RGO:12597 prostaglandin periostosis RGO:12597 anterior rib cupping RGO:12599 symmetrical anterior rib flaring RGO:12599 RGO:12605 high aortic obstruction RGO:12605 RGO:12607 subclavian artery obstruction RGO:12607 RGO:12608 pulmonary oligemia RGO:12608 chest wall arteriovenous fistula intercostal arteriovenous fistula RGO:12612 arteriovenous fistula of chest wall RGO:12612 ORDO:2038 SNOMEDCT:111289009 RGO:12613 pulmonary arteriovenous fistula RGO:12613 RGO:12618 indwelling catheter RGO:12618 superior rib notching RGO:12619 notching of the superior rib margins RGO:12619 RGO:12623 intercostal muscle atrophy in restrictive lung disease RGO:12623 RGO:12625 rib lesion in a child RGO:12625 ICD10CM:Q76.5 SNOMEDCT:72535009 RGO:12628 cervical rib RGO:12628 RGO:12634 granulomatous disease of childhood RGO:12634 RGO:12637 mesenchymal hamartoma of chest wall RGO:12637 short lesion of a rib RGO:12643 short rib lesion RGO:12643 long lesion of a rib RGO:12651 long rib lesion RGO:12651 RGO:12657 multiple expanding rib lesions RGO:12657 RGO:12662 mesenchymal hamartomas of chest wall RGO:12662 pigeon breast HP:0000768 ICD10CM:Q67.7 SNOMEDCT:38774000 RGO:12667 pectus carinatum RGO:12667 funnel chest HP:0000767 ICD10CM:Q67.6 SNOMEDCT:391987005 RGO:12672 pectus excavatum RGO:12672 RGO:12674 trauma with flail chest RGO:12674 RGO:12677 congenital fusion anomaly RGO:12677 RGO:12680 congenitally limited joint mobility RGO:12680 RGO:12684 radioulnar synostosis syndromes RGO:12684 RGO:12688 familial dwarfism with stiff joints RGO:12688 SNOMEDCT:702447002 RGO:12689 Kuskokwim syndrome RGO:12689 DOID:0110633 ORDO:97244 RGO:12694 rigid spine syndrome RGO:12694 RGO:12700 joint hypermobility syndrome RGO:12700 RGO:12704 congenital joint subluxation RGO:12704 SNOMEDCT:9634000 RGO:12705 congenital dislocation of radial head RGO:12705 chromosome 22 trisomy/tetrasomy ORDO:195 RGO:12710 cat-eye syndrome RGO:12710 DOID:9248 ORDO:672 SNOMEDCT:56677004 RGO:12725 Pallister-Hall syndrome RGO:12725 RGO:12732 monoarticular joint disease RGO:12732 RGO:12736 regional migratory osteoporosis of the legs RGO:12736 RGO:12741 transient osteoporosis of the hips RGO:12741 ORDO:53715 RADLEX:RID5202 SNOMEDCT:61778004 RGO:12742 tumoral calcinosis RGO:12742 RGO:12743 polyarticular joint disease RGO:12743 arthritis post-rheumatic fever RGO:12750 Jaccoud arthritis RGO:12750 DOID:11729 ICD10CM:A69.2 ORDO:91546 SNOMEDCT:23502006 RGO:12751 Lyme disease RGO:12751 RGO:12754 male-predominant arthritis RGO:12754 DOID:2092 SNOMEDCT:6011000119108 RGO:12756 transient arthritis RGO:12756 SNOMEDCT:239780003 RGO:12758 viral arthritis RGO:12758 RGO:12759 rheumatoid-like arthritis RGO:12759 enteropathic arthropathy SNOMEDCT:9350004 RGO:12762 enteropathic arthritis RGO:12762 degenerative joint disease in a young adult HP:0003088 RGO:12767 premature osteoarthritis RGO:12767 RADLEX:RID3559 RGO:12769 erosive osteoarthritis RGO:12769 RGO:12774 congenital bone dysplasias RGO:12774 RGO:12777 secondary osteoarthritis of the hip RGO:12777 RGO:12778 avascular necrosis of femoral head RGO:12778 HP:0008807 RGO:12783 acetabular dysplasia RGO:12783 RADLEX:RID5353 SNOMEDCT:362969004 RGO:12784 endocrine disorder RGO:12784 Charcot joint HP:0002821 ICD10CM:M14.6 SNOMEDCT:67536000 RGO:12785 neuropathic arthropathy RGO:12785 tabes DOID:10027 ICD10CM:A52.11 SNOMEDCT:316841006 RGO:12787 tabes dorsalis RGO:12787 HP:0100758 SNOMEDCT:36024000 SNOMEDCT:372070002 RGO:12792 gangrene RGO:12792 RGO:12796 myelopathy of pernicious anemia RGO:12796 SNOMEDCT:126962006 RGO:12797 neoplasm of spinal cord RGO:12797 RGO:12799 symmetrical sacroiliac joint disease RGO:12799 IBD DOID:0050589 HP:0002037 RADLEX:RID3474 SNOMEDCT:24526004 RGO:12800 inflammatory bowel disease RGO:12800 RGO:12801 asymmetrical sacroiliac joint disease RGO:12801 RGO:12802 unilateral sacroiliac joint disease RGO:12802 RGO:12803 narrowed joint space RGO:12803 RGO:12809 widened joint space RGO:12809 RGO:12810 congenital joint laxity or subluxation RGO:12810 RGO:12818 inflammatory synovial thickening RGO:12818 RGO:12820 neuropathic arthropathy atrophic type RGO:12820 SNOMEDCT:387637008 RGO:12821 joint effusion RGO:12821 RGO:12829 arthritis with osteoporosis RGO:12829 AIDS-associated arthritis RGO:12831 HIV-associated arthritis RGO:12831 RGO:12837 arthritis without osteoporosis RGO:12837 RGO:12841 arthritis with subluxation RGO:12841 RGO:12845 arthritis with swan-neck deformity RGO:12845 RGO:12846 arthritis with new bone formation RGO:12846 RGO:12852 plantar calcaneal spur RGO:12852 DOID:9600 ICD10CM:M72.2 SNOMEDCT:202882003 RGO:12854 plantar fasciitis RGO:12854 RGO:12856 calcaneal bone resorption RGO:12856 RGO:12858 arthritis with soft-tissue nodules RGO:12858 RGO:12861 juxta-articular soft-tissue mass RGO:12861 RGO:12865 calcific tendonitis RGO:12865 RGO:12871 synovial hypertrophy secondary to arthritis RGO:12871 DOID:2001 HP:0030430 SNOMEDCT:25169009 SNOMEDCT:443892003 RGO:12878 neuroma RGO:12878 RGO:12881 synovial hemangioma RGO:12881 popliteal cyst RADLEX:RID3892 RGO:12883 Baker cyst RGO:12883 RGO:12889 benign synovial lesion RGO:12889 RGO:12892 synovial hypertrophy secondary to arthritis or infection RGO:12892 RGO:12895 intracapsular chondroma RGO:12895 RGO:12896 joint-crossing bone lesion RGO:12896 RGO:12902 multiple intra-articular filling defects RGO:12902 DOID:2703 HP:0100769 RADLEX:RID3630 SNOMEDCT:416209007 RGO:12904 synovitis RGO:12904 RGO:12906 gouty tophi RGO:12906 SNOMEDCT:447059009 RGO:12907 lipoma arborescens RGO:12907 RGO:12909 calcified intra-articular body RGO:12909 RGO:12911 fragmented meniscus RGO:12911 calcification in articular cartilage DOID:1156 HP:0000934 RADLEX:RID5398 SNOMEDCT:239838005 RGO:12919 chondrocalcinosis RGO:12919 DOID:8398 SNOMEDCT:396275006 RGO:12924 degenerative arthritis RGO:12924 HP:0010886 RADLEX:RID5381 SNOMEDCT:82562007 RGO:12927 osteochondrosis dissecans RGO:12927 RGO:12932 calcinosis interstitialis universalis RGO:12932 RGO:12955 widespread soft-tissue calcification RGO:12955 SNOMEDCT:66924005 RGO:12962 calcinosis universalis RGO:12962 SNOMEDCT:17383000 RGO:12964 carbon monoxide poisoning RGO:12964 RGO:12973 localized soft-tissue calcification RGO:12973 RGO:12975 fracture with avulsed fragment RGO:12975 DOID:305 SNOMEDCT:71298006 RGO:12981 epithelioma RGO:12981 SNOMEDCT:37058002 RGO:12982 foreign body granuloma RGO:12982 Singleton-Merten dysplasia SNOMEDCT:254114000 RGO:12988 Singleton-Merten syndrome RGO:12988 calcification in bursa RGO:12989 bursal calcification RGO:12989 RGO:12990 bursal osteochondromatosis RGO:12990 RGO:12991 calcific bursitis RGO:12991 RGO:13001 nerve calcification RGO:13001 HP:0004934 RADLEX:RID34253 SNOMEDCT:237897009 RGO:13002 vascular calcification RGO:13002 SNOMEDCT:69742007 RGO:13004 Mönckeberg medial sclerosis RGO:13004 HP:0004416 RGO:13006 premature atherosclerosis RGO:13006 RGO:13009 calcification about the fingertips RGO:13009 RGO:13012 calcification in lymph nodes RGO:13012 SNOMEDCT:42284007 RGO:13013 BCG vaccination RGO:13013 RGO:13017 solitary large calcified soft tissue mass adjacent to bone RGO:13017 ORDO:199260 SNOMEDCT:703612005 SNOMEDCT:703614006 RGO:13022 calcifying aponeurotic fibroma RGO:13022 RGO:13030 osteoma or juxtacortical chondroma RGO:13030 RGO:13033 soft-tissue mass with adjacent bone erosion RGO:13033 RGO:13036 carcinoma of skin or mouth RGO:13036 DOID:8717 HP:0012399 RGO:13037 decubitus ulcer RGO:13037 DOID:2647 SNOMEDCT:128786009 SNOMEDCT:404086000 RGO:13049 parachordoma RGO:13049 RGO:13055 surfer knot RGO:13055 RGO:13058 musculoskeletal lesion with adjacent edema RGO:13058 DOID:9598 HP:0100537 RADLEX:RID3446 SNOMEDCT:36948007 RGO:13059 fasciitis RGO:13059 RGO:13064 soft tissue metastasis RGO:13064 DOID:2965 HP:0025232 RADLEX:RID3632 SNOMEDCT:84017003 RGO:13065 bursitis RGO:13065 RGO:13068 T2-hypointense musculoskeletal lesion RGO:13068 DFSP DOID:3507 ORDO:31112 SNOMEDCT:276799004 SNOMEDCT:76594008 RGO:13069 dermatofibrosarcoma protuberans RGO:13069 DOID:4233 RADLEX:RID4557 SNOMEDCT:271944004 SNOMEDCT:402561003 RGO:13074 clear cell sarcoma RGO:13074 RGO:13075 extensively mineralized mass RGO:13075 rhabdomyoblastoma DOID:2411 RADLEX:RID4437 SNOMEDCT:12169001 SNOMEDCT:404035005 RGO:13076 granular cell tumor RGO:13076 DOID:3777 ICD10CM:L92.0 SNOMEDCT:65508009 RGO:13077 granuloma annulare RGO:13077 SNOMEDCT:25889007 RGO:13083 benign fibrous histiocytoma RGO:13083 DOID:7327 ICD10CM:M72.4 SNOMEDCT:400138001 SNOMEDCT:703616008 RGO:13084 nodular fasciitis RGO:13084 ORDO:247762 SNOMEDCT:400102008 SNOMEDCT:420777000 SNOMEDCT:63629005 RGO:13086 lipoblastoma RGO:13086 DOID:4239 HP:0012218 ORDO:163699 SNOMEDCT:404056007 SNOMEDCT:88195001 RGO:13093 alveolar soft part sarcoma RGO:13093 DOID:6193 ORDO:293202 SNOMEDCT:59238007 RGO:13095 epithelioid sarcoma RGO:13095 RGO:13096 extraskeletal Ewing sarcoma RGO:13096 RGO:13098 round-cell soft-tissue lesion RGO:13098 RGO:13101 soft-tissue tumor in a child RGO:13101 DOID:4415 RADLEX:RID4304 SNOMEDCT:25889007 RGO:13102 fibrous histiocytoma RGO:13102 RGO:13103 soft-tissue tumor in a young adult RGO:13103 RGO:13105 soft-tissue tumor in an older adult RGO:13105 RGO:13108 subcutaneous tumor RGO:13108 RGO:13109 angiomatous lesion RGO:13109 RGO:13111 skin appendage tumors RGO:13111 RGO:13113 intermuscular soft-tissue tumor RGO:13113 DOID:6496 ORDO:209916 SNOMEDCT:404079008 RGO:13116 extraskeletal myxoid chondrosarcoma RGO:13116 RGO:13118 intramuscular soft-tissue tumor RGO:13118 RGO:13121 rhabdmyosarcoma RGO:13121 RGO:13122 intra-articular or juxta-articular soft-tissue tumor RGO:13122 RGO:13125 multifocal soft-tissue tumor RGO:13125 RGO:13131 soft-tissue tumor with associated calcification RGO:13131 DOID:2667 SNOMEDCT:38406003 RGO:13134 benign mesenchymoma RGO:13134 DOID:5758 SNOMEDCT:89623007 RGO:13140 malignant mesenchymoma RGO:13140 RGO:13142 cystic soft-tissue tumor RGO:13142 RADLEX:RID13399 SNOMEDCT:13351007 SNOMEDCT:182483003 RGO:13143 bursa RGO:13143 RGO:13144 mucoid cyst RGO:13144 RADLEX:RID3940 SNOMEDCT:123250005 SNOMEDCT:240205003 RGO:13148 synovial cyst RGO:13148 DOID:876 ICD10CM:M60.0 SNOMEDCT:65110003 RGO:13149 tropical pyomyositis RGO:13149 RGO:13150 soft-tissue tumor with fluid-fluid level RGO:13150 SNOMEDCT:128744003 RGO:13151 angiomatoid fibrous histiocytoma RGO:13151 RGO:13154 soft-tissue tumor with prominent vascularity RGO:13154 HP:0003199 RGO:13170 decreased muscle mass RGO:13170 SNOMEDCT:240080003 RGO:13175 benign congenital hypotonia RGO:13175 HP:0003758 RGO:13177 decreased subcutaneous fat RGO:13177 RGO:13179 increased muscle mass RGO:13179 RGO:13180 exercise hypertrophy RGO:13180 SNOMEDCT:66042003 RGO:13181 congenital muscular hypertrophy RGO:13181 muscular dystrophy Duchenne type pseudohypertrophic muscular dystrophy DOID:11723 ORDO:98896 SNOMEDCT:76670001 RGO:13183 Duchenne muscular dystrophy RGO:13183 RGO:13184 increased subcutaneous fat RGO:13184 SNOMEDCT:415530009 RGO:13185 exogenous obesity RGO:13185 RGO:13186 thick heel pad RGO:13186 SNOMEDCT:372659008 SNOMEDCT:40556005 RGO:13191 hydantoin RGO:13191 SNOMEDCT:87923000 RGO:13193 occupational RGO:13193 RGO:13194 soft-tissue gas RGO:13194 RGO:13200 increased soft-tissue interstitial markings RGO:13200 lymphatic vessel dysplasia RADLEX:RID3327 SNOMEDCT:48087001 RGO:13208 lymphangiectasia RGO:13208 RGO:13217 metastases to lymph nodes RGO:13217 RGO:13227 lymph node filling defect RGO:13227 RGO:13231 fatty replacement of lymph node RGO:13231 RGO:13232 normal anatomic hilum RGO:13232 DOID:1682 HP:0002564 SNOMEDCT:13213009 RGO:13234 congenital heart disease RGO:13234 chondroectodermal dysplasia mesoectodermal dysplasia DOID:12714 ICD10CM:Q77.6 ORDO:289 SNOMEDCT:62501005 RGO:13238 Ellis-van Creveld syndrome RGO:13238 rubella infection in utero DOID:9228 ICD10CM:P35.0 ORDO:290 SNOMEDCT:1857005 RGO:13240 congenital rubella syndrome RGO:13240 ORDO:97214 SNOMEDCT:445928005 RGO:13242 Eisenmenger syndrome RGO:13242 DOID:12705 ORDO:95 RADLEX:RID5152 SNOMEDCT:10394003 RGO:13244 Friedreich ataxia RGO:13244 DOID:2352 ICD10CM:E83.11 RADLEX:RID5205 SNOMEDCT:399187006 RGO:13246 hemochromatosis RGO:13246 cretinism SNOMEDCT:217710005 RGO:13251 infantile hypothyroidism RGO:13251 DOID:0050144 SNOMEDCT:42402006 RGO:13253 Kartagener syndrome RGO:13253 XXY syndrome chromosome XXY syndrome DOID:1921 SNOMEDCT:22053006 RGO:13254 Klinefelter syndrome RGO:13254 DOID:2738 ORDO:758 RADLEX:RID3271 SNOMEDCT:252246005 RGO:13262 pseudoxanthoma elasticum RGO:13262 Bourneville disease TS DOID:13515 ICD10CM:Q85.1 ORDO:805 RADLEX:RID34754 SNOMEDCT:7199000 RGO:13265 tuberous sclerosis RGO:13265 DOID:0050461 HP:0012068 ICD10CM:E77.1 ORDO:93 SNOMEDCT:54954004 RGO:13272 aspartylglucosaminuria RGO:13272 DOID:1935 ORDO:110 SNOMEDCT:5619004 RGO:13273 Bardet-Biedl syndrome RGO:13273 Cassidy-Scholte syndrome Thorson-Bioerck syndrome argentaffinoma syndrome DOID:8600 ICD10CM:E34.0 SNOMEDCT:35868009 RGO:13274 carcinoid syndrome RGO:13274 Cayler syndrome SNOMEDCT:51409009 RGO:13275 cardiofacial syndrome RGO:13275 cat cry syndrome cri du chat syndrome RGO:13278 chromosome 5:del(5p) syndrome RGO:13278 DOID:3144 HP:0000973 ORDO:209 SNOMEDCT:58588007 RGO:13280 cutis laxa RGO:13280 deaf mutism RGO:13281 deaf-mutism RGO:13281 CATCH 22 DGS DiGeorge anomaly DiGeorge sequence third and fourth pharyngeal pouch syndrome DOID:11198 SNOMEDCT:77128003 RGO:13283 DiGeorge syndrome RGO:13283 African myocardiopathy DOID:12932 HP:0006685 ORDO:75565 RADLEX:RID3256 SNOMEDCT:398716006 RGO:13285 endomyocardial fibrosis RGO:13285 DOID:14499 ORDO:324 SNOMEDCT:16652001 RGO:13286 Fabry disease RGO:13286 Dilantin embryopathy congenital hydantoin syndrome fetal dilantin syndrome phenytoin embryopathy ICD10CM:Q86.1 ORDO:1912 SNOMEDCT:70065001 RGO:13288 fetal hydantoin syndrome RGO:13288 Kawasaki disease mucocutaneous lymph node syndrome ORDO:2331 SNOMEDCT:75053002 RGO:13294 Kawasaki syndrome RGO:13294 RGO:13296 Kugelberg-Welander syndrome RGO:13296 DOID:1998 SNOMEDCT:204319006 RGO:13298 Lutembacher syndrome RGO:13298 DOID:0050765 SNOMEDCT:66881004 RGO:13300 neuroacanthocytosis RGO:13300 RGO:13306 Shone-Edwards complex RGO:13306 RGO:13310 sternal malformation RGO:13310 ORDO:3205 RADLEX:RID34788 SNOMEDCT:19886006 RGO:13311 Sturge-Weber syndrome RGO:13311 thrombocytopenia-absent radius syndrome SNOMEDCT:85589009 RGO:13312 TAR syndrome RGO:13312 RGO:13313 thoracoabdominal wall defect syndrome RGO:13313 DOID:12583 SNOMEDCT:83092002 RGO:13318 velocardiofacial syndrome RGO:13318 pulmonary stenosis HP:0001642 SNOMEDCT:56786000 RGO:13327 pulmonic stenosis RGO:13327 UVH cor triloculare biatriatum double-inlet left ventricle univentricular heart HP:0001750 ICD10CM:Q20.4 SNOMEDCT:45503006 RGO:13330 single ventricle RGO:13330 AV canal defect DOID:0050651 HP:0006695 RGO:13331 atrioventricular canal defect RGO:13331 HP:0010883 RGO:13333 aortic atresia RGO:13333 DOID:14289 ORDO:1880 RADLEX:RID34612 RGO:13335 Ebstein anomaly RGO:13335 DOID:12929 HP:0001706 ICD10CM:I42.4 SNOMEDCT:65457005 RGO:13336 endocardial fibroelastosis RGO:13336 RGO:13338 heart failure in the first week of life RGO:13338 SNOMEDCT:275519006 RGO:13346 peripheral arteriovenous malformation RGO:13346 RGO:13347 heart failure in the first month of life RGO:13347 HP:0011565 SNOMEDCT:253276007 RGO:13354 common atrium RGO:13354 triatrial heart HP:0010774 ICD10CM:Q24.2 SNOMEDCT:55510008 RGO:13356 cor triatriatum RGO:13356 HP:0011660 RGO:13359 hemitruncus RGO:13359 HP:0010954 ICD10CM:Q22.6 RGO:13362 hypoplastic right heart syndrome RGO:13362 TAPVR below the diaphragm RGO:13370 total anomalous pulmonary venous return below the diaphragm RGO:13370 DORV DOID:6406 HP:0001719 ICD10CM:Q20.1 ORDO:3426 SNOMEDCT:7484005 RGO:13383 double outlet right ventricle RGO:13383 HP:0006521 RGO:13394 pulmonary lymphangiectasia RGO:13394 RGO:13396 left-to-right shunt in congenital heart disease RGO:13396 ASD interatrial communication interauricular communication DOID:1882 HP:0001631 ICD10CM:Q21.1 RADLEX:RID38590 SNOMEDCT:70142008 RGO:13397 atrial septal defect RGO:13397 PDA DOID:13832 HP:0001643 ICD10CM:Q25.0 ORDO:706 RADLEX:RID4975 SNOMEDCT:83330001 RGO:13399 patent ductus arteriosus RGO:13399 HP:0011604 ICD10CM:Q21.4 RADLEX:RID1444 SNOMEDCT:17024001 RGO:13401 aortopulmonary window RGO:13401 RGO:13404 corrected transposition of great vessels with VSD RGO:13404 RGO:13406 left ventricular-right atrial shunt RGO:13406 RGO:13408 ruptured sinus of Valsalva aneurysm into right heart RGO:13408 pink tetralogy of Fallot RGO:13410 acyanotic tetralogy of Fallot RGO:13410 RGO:13412 right-to-left shunt or admixture lesion in congenital heart disease RGO:13412 TGV transposition of great arteries HP:0001669 RADLEX:RID34661 SNOMEDCT:204296002 RGO:13415 transposition of great vessels RGO:13415 Ebstein anomaly with atrial septal defect RGO:13417 Ebstein anomaly with ASD RGO:13417 HP:0006548 SNOMEDCT:303070000 RGO:13419 pulmonary arteriovenous malformation RGO:13419 SNOMEDCT:204467000 RGO:13420 pulmonary vein atresia RGO:13420 RGO:13421 right pulmonary artery fistula to left atrium RGO:13421 RGO:13422 trilogy of Fallot RGO:13422 RGO:13424 marked cyanosis in first week of life RGO:13424 aortic arch interruption ICD10CM:Q25.21 ORDO:2299 RGO:13426 interruption of aortic arch RGO:13426 DOID:13042 HP:0011726 ICD10CM:P29.3 RADLEX:RID4974 SNOMEDCT:206597007 RGO:13427 persistent fetal circulation RGO:13427 RGO:13429 mild or intermittent cyanosis in first week RGO:13429 RGO:13432 late onset of cyanosis in neonatal congenital heart disease RGO:13432 RGO:13433 double outlet right ventricle with pulmonary stenosis RGO:13433 RGO:13434 single ventricle with pulmonary stenosis RGO:13434 RGO:13437 right-to-left atrial shunt RGO:13437 RGO:13439 transposition of great vessels with interatrial communication RGO:13439 RGO:13440 atrial septal defect with communication of left superior vena cava to left atrium RGO:13440 RGO:13442 normal newborn with patent foramen ovale RGO:13442 ICD10CM:Q21.8 SNOMEDCT:204306007 RGO:13443 pentalogy of Fallot RGO:13443 HP:0011565 RGO:13446 single atrium RGO:13446 RGO:13447 tricuspid stenosis with interatrial communication RGO:13447 parchment RV ORDO:3403 RADLEX:RID34741 RGO:13448 Uhl anomaly RGO:13448 RGO:13449 complicated atrial shunt RGO:13449 HP:0011641 SNOMEDCT:373093003 RGO:13454 coronary artery fistula RGO:13454 RGO:13458 right-to-left ventricular shunt RGO:13458 RGO:13459 complete transposition of great vessels with ventricular septal defect RGO:13459 RGO:13462 corrected transposition of great vessels with ventricular septal defect and marked pulmonic stenosis RGO:13462 VSD DOID:1657 HP:0001629 ICD10CM:Q21.0 ORDO:1480 ORDO:99097 RADLEX:RID3277 SNOMEDCT:30288003 RGO:13463 ventricular septal defect RGO:13463 HP:0011581 ICD10CM:Q20.2 ORDO:3427 SNOMEDCT:7368005 RGO:13466 double outlet left ventricle RGO:13466 SNOMEDCT:26146002 RGO:13468 complete transposition of great vessels RGO:13468 SNOMEDCT:83799000 RGO:13471 corrected transposition of great vessels RGO:13471 HP:0001683 SNOMEDCT:78250005 RGO:13472 ectopia cordis RGO:13472 aneurysm of sinus of Valsalva HP:0011645 SNOMEDCT:54160000 RGO:13475 sinus of Valsalva aneurysm RGO:13475 AV communis CAVC complete AV canal ORDO:1329 RGO:13476 complete atrioventricular canal RGO:13476 RGO:13478 right-to-left shunt at ductus level RGO:13478 ORDO:99054 RGO:13486 pulmonary valvular stenosis RGO:13486 HP:0001682 SNOMEDCT:204368006 RGO:13489 subaortic stenosis RGO:13489 RGO:13493 acyanotic congenital heart disease with normal pulmonary vascularity RGO:13493 ALCAPA RGO:13495 anomalous left coronary artery from pulmonary artery RGO:13495 AI AR aortic regurgitation aortic valve insufficiency HP:0001659 SNOMEDCT:60234000 RGO:13496 aortic insufficiency RGO:13496 IHSS subvalvular aortic stenosis SNOMEDCT:360465008 RGO:13497 idiopathic hypertrophic subaortic stenosis RGO:13497 RGO:13498 interruption of aortic arch with VSD and PDA RGO:13498 mitral regurgitation HP:0001653 SNOMEDCT:48724000 RGO:13499 mitral insufficiency RGO:13499 RGO:13501 acyanotic congenital heart disease with increased pulmonary vascularity RGO:13501 RGO:13503 cyanotic congenital heart disease with increased pulmonary vascularity RGO:13503 RGO:13508 single ventricle without PS RGO:13508 RGO:13509 tricuspid atresia without PS RGO:13509 Eisenmenger physiology RGO:13510 cyanotic congenital heart disease with precapillary hypertension vascularity RGO:13510 RGO:13516 single ventricle without pulmonary stenosis RGO:13516 RGO:13519 congenital heart disease with decreased pulmonary vascularity RGO:13519 RGO:13521 double outlet right ventricle with PS RGO:13521 RGO:13524 single ventricle with PS RGO:13524 HP:0005180 SNOMEDCT:111287006 RGO:13527 tricuspid insufficiency RGO:13527 RGO:13535 single ventricle with transposition of great vessels RGO:13535 RGO:13538 aortic arch anomaly RGO:13538 SNOMEDCT:70602002 RGO:13540 pseudocoarctation of aorta RGO:13540 RGO:13543 anomalous left common carotid artery RGO:13543 RGO:13545 innominate artery compression syndrome RGO:13545 RGO:13546 left aortic arch with right ductus and right descending aorta RGO:13546 RGO:13548 right aortic arch with left descending aorta RGO:13548 type 3 aortic arch RGO:13549 right aortic arch with right descending aorta and aberrant left subclavian artery RGO:13549 RGO:13550 congenital heart disease with anterior right aortic arch RGO:13550 RGO:13554 transposition of great vessels with VSD and PS RGO:13554 RGO:13557 anomalous thoracic arterial communication RGO:13557 RGO:13560 pseudotruncus RGO:13560 RGO:13562 anomalous origin of systemic artery RGO:13562 ORDO:1138 SNOMEDCT:68092007 RGO:13564 anomalous origin of pulmonary artery RGO:13564 RGO:13565 anomalous pulmonary artery arising from aorta RGO:13565 RGO:13577 abnormal position of the heart RGO:13577 RGO:13581 congenital absence of left pericardium RGO:13581 DOID:9565 HP:0001651 ICD10CM:Q24.0 ORDO:1666 SNOMEDCT:27637000 RGO:13596 dextrocardia RGO:13596 HP:0030718 SNOMEDCT:67751000119106 RGO:13602 right atrial enlargement RGO:13602 RADLEX:RID34796 SNOMEDCT:128404006 RGO:13605 right heart failure RGO:13605 RGO:13609 coronary artery fistula to right atrium RGO:13609 DOID:9955 ICD10CM:Q23.4 ORDO:2248 RADLEX:RID34704 SNOMEDCT:62067003 RGO:13612 hypoplastic left heart syndrome RGO:13612 RGO:13614 post-mitral valve replacement RGO:13614 HP:0004935 SNOMEDCT:448564004 RGO:13615 pulmonary atresia RGO:13615 DOID:5644 HP:0001704 ORDO:95458 SNOMEDCT:253383003 RGO:13622 tricuspid valve prolapse RGO:13622 RGO:13623 right ventricular enlargement RGO:13623 SNOMEDCT:268180007 RGO:13628 pseudotruncus arteriosus RGO:13628 RGO:13635 filling defect in right ventricle RGO:13635 blood clot clot thrombosis RADLEX:RID5037 SNOMEDCT:396339007 RGO:13637 thrombus RGO:13637 RGO:13639 anomalous muscle bundle RGO:13639 RGO:13644 prolapsed valve RGO:13644 HP:0005162 ICD10CM:I50.1 SNOMEDCT:85232009 RGO:13645 left ventricular failure RGO:13645 RGO:13651 mitral anulus anomaly RGO:13651 RGO:13653 papillary muscle rupture RGO:13653 HP:0011571 RGO:13654 parachute mitral valve complex RGO:13654 MVP DOID:988 HP:0001634 RADLEX:RID3269 SNOMEDCT:409712001 RGO:13658 mitral valve prolapse RGO:13658 DOID:14056 SNOMEDCT:48872007 RGO:13662 rheumatic endocarditis RGO:13662 RGO:13663 ruptured chordae tendineae RGO:13663 SNOMEDCT:1131009 SNOMEDCT:396352002 RGO:13664 congenital valvular insufficiency RGO:13664 extra bump along upper left heart silhouette RADLEX:RID35630 RGO:13669 third mogul sign RGO:13669 RGO:13682 right atrial appendage, levoposition RGO:13682 RGO:13685 left ventricular enlargement RGO:13685 RGO:13697 neoplasm of left ventricle RGO:13697 ORDO:1208 SNOMEDCT:253590009 RGO:13699 pulmonary atresia with intact ventricular septum RGO:13699 RGO:13700 subvalvular left ventricular aneurysm RGO:13700 ORDO:99071 RGO:13707 aorta-left ventricle tunnel RGO:13707 RGO:13710 blunt chest trauma RGO:13710 RGO:13711 myxomatous degeneration of aortic valve RGO:13711 RGO:13716 high ventricular septal defect with prolapsed noncoronary aortic cusp RGO:13716 RGO:13717 prosthetic valve regurgitation RGO:13717 RGO:13718 degeneration of nonbiological valve component RGO:13718 RGO:13720 strut fracture RGO:13720 RGO:13721 suture line dehiscence RGO:13721 RGO:13722 thrombosis of prosthesis RGO:13722 DOID:10763 HP:0000822 RADLEX:RID39097 SNOMEDCT:38341003 RGO:13723 hypertension RGO:13723 RADLEX:RID3235 SNOMEDCT:414545008 RGO:13732 ischemic heart disease RGO:13732 HP:0001677 HP:0004929 SNOMEDCT:443502000 RGO:13733 coronary atherosclerosis RGO:13733 SNOMEDCT:23687008 RGO:13735 coronary spasm RGO:13735 aneurysm of left ventricle SNOMEDCT:297160003 RGO:13740 left ventricular aneurysm RGO:13740 high-flow heart syndrome hyperkinetic circulatory state RGO:13743 high-output heart function RGO:13743 myocardiopathy DOID:0050700 HP:0001638 ICD10CM:I42 RADLEX:RID3243 SNOMEDCT:85898001 RGO:13752 cardiomyopathy RGO:13752 RGO:13755 idiopathic dilated cardiomyopathy RGO:13755 congenital myocardiopathy ICD10CM:I42.4 RGO:13765 congenital cardiomyopathy RGO:13765 grossly enlarged heart RGO:13774 massive cardiomegaly RGO:13774 HP:0025406 SNOMEDCT:13791008 RGO:13784 asthenia RGO:13784 SNOMEDCT:62286002 RGO:13787 senile atrophy RGO:13787 RGO:13791 cardiac or pericardial neoplasm or cyst RGO:13791 SNOMEDCT:253734000 RGO:13801 pericardial diverticulum RGO:13801 ORDO:2022 RGO:13813 endomyocardial fibroelastosis RGO:13813 ICD10CM:I31.1 RGO:13823 pericardial calcification RGO:13823 ICD10CM:I31.1 SNOMEDCT:52535005 RGO:13824 chronic constrictive pericarditis RGO:13824 RGO:13825 idiopathic pericarditis RGO:13825 ICD10CM:I30.1 RGO:13826 purulent pericarditis RGO:13826 DOID:11482 HP:0011851 SNOMEDCT:23412002 RGO:13828 hemopericardium RGO:13828 DOID:1586 ORDO:3099 SNOMEDCT:58718002 RGO:13829 rheumatic fever RGO:13829 RGO:13830 gas embolism RGO:13830 HP:0003826 SNOMEDCT:276507005 RGO:13831 fetal death RGO:13831 RGO:13835 resuscitation maneuver RGO:13835 RGO:13838 abscess perforation into vessel RGO:13838 RGO:13839 asthmatic episode RGO:13839 whooping cough DOID:1116 RADLEX:RID34768 SNOMEDCT:27836007 RGO:13850 pertussis RGO:13850 DOID:113 RADLEX:RID28524 SNOMEDCT:82542004 RGO:13851 pneumopericardium RGO:13851 RGO:13853 congenital absence of the pericardium with pneumothorax RGO:13853 RGO:13856 pericarditis due to gas-forming organism RGO:13856 DOID:14044 SNOMEDCT:28381002 RGO:13865 rheumatic pericarditis RGO:13865 SNOMEDCT:123598000 RGO:13882 polyserositis RGO:13882 DOID:0050426 ICD10CM:L51.1 ORDO:36426 SNOMEDCT:73442001 RGO:13884 Stevens-Johnson syndrome RGO:13884 RGO:13892 generalized pulmonary arterial hypervascularity RGO:13892 RGO:13894 rupture of sinus of Valsalva aneurysm RGO:13894 ORDO:2037 RGO:13895 aorta-pulmonary artery fistula RGO:13895 SNOMEDCT:81990004 RGO:13897 cor biloculare RGO:13897 RGO:13898 double outlet right ventricle without PS RGO:13898 ICD10CM:Q20.1 ORDO:101042 SNOMEDCT:7484005 RGO:13900 Taussig-Bing syndrome RGO:13900 increased pulmonary arterial circulation to one lung unilaterally increased pulmonary arterial circulation RGO:13902 unilateral pulmonary arterial hypervascularity RGO:13902 RGO:13910 large main pulmonary artery RGO:13910 HP:0004937 SNOMEDCT:194892009 RGO:13911 pulmonary artery aneurysm RGO:13911 HP:0005134 SNOMEDCT:6996004 RGO:13922 absent pulmonary valve RGO:13922 RGO:13923 aortopulmonary fistula RGO:13923 HP:0011629 ORDO:99129 RGO:13925 congenital absence of the pericardium RGO:13925 HP:0010444 RGO:13929 pulmonary insufficiency RGO:13929 RGO:13930 tricuspid atresia without pulmonary stenosis RGO:13930 RGO:13936 high altitude dwelling RGO:13936 RGO:13938 pleural fibrothorax RGO:13938 SNOMEDCT:87153008 RGO:13940 alveolar microlithiasis RGO:13940 RGO:13942 bronchioloalveolar cell carcinoma RGO:13942 DOID:9563 HP:0002110 ICD10CM:J47 RADLEX:RID28496 SNOMEDCT:12295008 RGO:13943 bronchiectasis RGO:13943 RADLEX:RID4839 SNOMEDCT:212372004 RGO:13946 fat embolism RGO:13946 RADLEX:RID3821 SNOMEDCT:125565008 RGO:13947 interstitial fibrosis RGO:13947 RGO:13956 chronic left ventricular failure RGO:13956 HP:0030950 RGO:13961 pulmonary venous hypertension RGO:13961 RGO:13962 ventriculoatrial shunt for hydrocephalus RGO:13962 RGO:13972 localized pulmonary vessel enlargement RGO:13972 RGO:13977 anomalous insertion of pulmonary vein into left atrium RGO:13977 DOID:11294 SNOMEDCT:14156004 SNOMEDCT:233982006 RGO:13981 cirsoid aneurysm RGO:13981 RGO:13986 tetralogy of Fallot with absent pulmonary valve RGO:13986 RGO:13987 main pulmonary artery obstruction RGO:13987 ICD10CM:Q25.71 SNOMEDCT:26780008 RGO:13992 coarctation of pulmonary artery RGO:13992 RGO:13998 generalized pulmonary arterial hypovascularity RGO:13998 HP:0002791 SNOMEDCT:31515003 RGO:14004 hypoventilation RGO:14004 HP:0011106 ICD10CM:E86.1 SNOMEDCT:28560003 RGO:14005 hypovolemia RGO:14005 RGO:14012 enlarged pulmonary veins RGO:14012 RGO:14019 obstruction of pulmonary veins RGO:14019 left-to-right shunt RGO:14021 systemic-to-pulmonary vascular shunt RGO:14021 RGO:14033 occlusion of pulmonary vein RGO:14033 DOID:11516 ICD10CM:I11 SNOMEDCT:64715009 RGO:14048 hypertensive heart disease RGO:14048 RGO:14056 tricuspid atresia without transposition RGO:14056 aneurysm of aorta DOID:3627 HP:0004942 SNOMEDCT:67362008 RGO:14057 aortic aneurysm RGO:14057 AML DOID:3314 HP:0006772 RADLEX:RID4343 SNOMEDCT:19929002 RGO:14062 angiomyolipoma RGO:14062 HP:0012180 SNOMEDCT:234021009 SNOMEDCT:42182000 RGO:14063 cystic medial necrosis RGO:14063 RADLEX:RID3328 SNOMEDCT:233991005 SNOMEDCT:51668007 RGO:14066 mycotic aneurysm RGO:14066 RGO:14069 post-stenotic aneurysm RGO:14069 RGO:14070 dissecting aneurysm of the ascending aorta or arch RGO:14070 HP:0030882 ICD10CM:I25.41 SNOMEDCT:50570003 RGO:14078 coronary artery aneurysm RGO:14078 SNOMEDCT:399980009 RGO:14081 necrotizing arteritis RGO:14081 RADLEX:RID4825 SNOMEDCT:55584005 RGO:14088 embolus RGO:14088 RGO:14094 atrial fibrillation with left atrial thrombus RGO:14094 RGO:14095 Chagas myocardiopathy with intracardiac thrombus RGO:14095 RGO:14096 myocardial infarction with left ventricular thrombus RGO:14096 RGO:14099 atherosclerosis with atheroma RGO:14099 CTD collagen disease DOID:65 SNOMEDCT:105969002 RGO:14102 connective tissue disease RGO:14102 RGO:14104 african idiopathic aortitis RGO:14104 SNOMEDCT:51510002 RGO:14105 ergotism RGO:14105 DOID:3103 ICD10CM:G54.0 ORDO:97330 RADLEX:RID3304 SNOMEDCT:128210009 RGO:14106 thoracic outlet syndrome RGO:14106 RGO:14107 vibratory tools RGO:14107 azygos vein dilatation RGO:14108 dilated azygos vein RGO:14108 SNOMEDCT:61688009 RGO:14115 overhydration RGO:14115 SVC obstruction SVC syndrome obstruction of SVC obstruction of superior vena cava superior vena cava obstruction HP:0031041 SNOMEDCT:63363004 RGO:14124 superior vena cava syndrome RGO:14124 SNOMEDCT:203222000 RGO:14137 osteomyelitis of clavicle RGO:14137 IVC obstruction obstruction of IVC obstruction of inferior vena cava RGO:14141 inferior vena cava obstruction RGO:14141 RGO:14149 pelvic varicosities RGO:14149 RGO:14152 web at junction of IVC and right atrium RGO:14152 IVC anomaly anomaly of IVC inferior vena cava anomaly ORDO:95499 RGO:14153 anomaly of inferior vena cava RGO:14153 absence of IVC absent IVC SNOMEDCT:204463001 RGO:14154 absence of inferior vena cava RGO:14154 bilateral venae cavae RGO:14156 bilateral cavae RGO:14156 SNOMEDCT:95233002 RGO:14159 retrocaval ureter RGO:14159 RGO:14162 catheter embolism RGO:14162 RADLEX:RID4877 SNOMEDCT:76676007 RGO:14163 extravasation RGO:14163 RGO:14165 malpositioned catheter RGO:14165 RADLEX:RID4827 SNOMEDCT:271376002 RGO:14169 air embolism RGO:14169 RGO:14173 subcutaneous or mediastinal emphysema RGO:14173 RGO:14174 thoracic duct laceration RGO:14174 air space pattern air-space disease air-space lung disease pulmonary consolidation RGO:14175 alveolar lung disease RGO:14175 RADLEX:RID34999 RGO:14178 air bronchogram RGO:14178 RGO:14179 butterfly distribution in lung RGO:14179 lung infarct lung infarction pulmonary infarct RADLEX:RID34889 SNOMEDCT:64662007 RGO:14191 pulmonary infarction RGO:14191 adenocarcinoma in situ RGO:14194 bronchiolo-alveolar carcinoma RGO:14194 paraffinoma SNOMEDCT:416916004 RGO:14197 lipoid pneumonia RGO:14197 HP:0040223 RADLEX:RID4709 SNOMEDCT:78144005 RGO:14204 pulmonary hemorrhage RGO:14204 ICD10CM:J70.0 SNOMEDCT:84004001 RGO:14205 radiation pneumonitis RGO:14205 RGO:14206 intralobar pulmonary sequestration RGO:14206 RGO:14208 pulmonary lobar enlargement RGO:14208 RGO:14212 chronic pulmonary lobar consolidation RGO:14212 DOID:8752 ICD10CM:A15.0 SNOMEDCT:80003002 RGO:14216 tuberculous pneumonia RGO:14216 ICD10CM:J98.09 SNOMEDCT:69921001 RGO:14223 broncholithiasis RGO:14223 HP:0002780 SNOMEDCT:54203008 RGO:14224 bronchomalacia RGO:14224 RADLEX:RID28494 SNOMEDCT:448370006 RGO:14237 rounded atelectasis RGO:14237 RGO:14245 inadequate drug therapy RGO:14245 HP:0031690 RGO:14248 opportunistic infection RGO:14248 RGO:14256 esophageal bronchus RGO:14256 RGO:14259 tracheal lesion RGO:14259 SNOMEDCT:48387007 RGO:14260 tracheostomy RGO:14260 RGO:14261 chronic aspiration pneumonia in a child RGO:14261 RGO:14268 acute disseminated airspace opacity RGO:14268 RGO:14274 chronic disseminated air-space opacity RGO:14274 HP:0006517 ICD10CM:J84.01 SNOMEDCT:10501004 RGO:14275 alveolar proteinosis RGO:14275 HP:0006532 SNOMEDCT:699014000 RGO:14278 recurrent pneumonia RGO:14278 DOID:11396 HP:0100598 ICD10CM:J81 RADLEX:RID4866 SNOMEDCT:19242006 RGO:14286 pulmonary edema RGO:14286 ICD10CM:O88.1 RADLEX:RID4841 SNOMEDCT:17263003 RGO:14300 amniotic fluid embolism RGO:14300 DIC disseminated intravascular coagulopathy RGO:14301 disseminated intravascular coagulation RGO:14301 DOID:13593 HP:0100601 ICD10CM:O15 SNOMEDCT:15938005 RGO:14302 eclampsia RGO:14302 SNOMEDCT:87588000 RGO:14305 high altitude RGO:14305 HP:0002781 RGO:14314 upper airway obstruction RGO:14314 RGO:14316 unilateral pulmonary edema RGO:14316 RGO:14319 unilateral lung contusion RGO:14319 RGO:14322 catheter malposition with infusion into pulmonary artery and lung RGO:14322 ARDS adult hyaline membrane disease adult respiratory distress syndrome ICD10CM:J80 ORDO:70578 RGO:14326 acute respiratory distress syndrome RGO:14326 RGO:14329 respirator lung RGO:14329 DOID:11394 SNOMEDCT:67782005 RGO:14331 shock lung RGO:14331 HP:0002835 RADLEX:RID10398 SNOMEDCT:14766002 SNOMEDCT:68052005 RGO:14333 aspiration RGO:14333 SNOMEDCT:242784006 SNOMEDCT:371708003 RGO:14334 electric shock RGO:14334 RGO:14337 insulin reaction RGO:14337 RGO:14339 near-strangulation RGO:14339 SNOMEDCT:125199004 SNOMEDCT:238456006 RGO:14341 snake bite RGO:14341 RGO:14342 acute lung injury and ards in children RGO:14342 SNOMEDCT:33499000 RGO:14345 oxygen toxicity RGO:14345 RGO:14352 bone marrow transplantation RGO:14352 RGO:14363 reverse butterfly pattern RGO:14363 RGO:14364 lung contusion RGO:14364 RGO:14368 pulmonary thromboembolism with multiple infarctions RGO:14368 RGO:14370 air-space opacity in leukemia or lymphoma RGO:14370 DOID:874 SNOMEDCT:53084003 RGO:14371 bacterial pneumonia RGO:14371 DOID:14477 RGO:14374 cytomegalovirus pneumonia RGO:14374 RGO:14380 ill-defined multifocal lung opacities RGO:14380 DOID:0050152 HP:0011951 SNOMEDCT:422588002 RGO:14382 aspiration pneumonia RGO:14382 RGO:14405 diffuse mixed airspace-interstitial lung disease RGO:14405 RGO:14407 pulmonary edema in heart failure or ARDS RGO:14407 DOID:9808 SNOMEDCT:50581000 RGO:14410 Goodpasture syndrome RGO:14410 end-stage interstitial pulmonary fibrosis end-stage lung disease HP:0025175 RADLEX:RID35280 RGO:14416 honeycomb lung RGO:14416 Kerley lines RGO:14420 acute diffuse fine reticular lung opacities RGO:14420 RGO:14427 chronic Kerley lines RGO:14427 RGO:14430 lymphangitic metastases RGO:14430 RGO:14443 miliary lung opacities RGO:14443 LIP RGO:14454 lymphocytic interstitial pneumonitis RGO:14454 DOID:5052 ORDO:31202 SNOMEDCT:428111003 RGO:14455 melioidosis RGO:14455 DOID:3319 SNOMEDCT:277844007 RGO:14459 pulmonary lymphangioleiomyomatosis RGO:14459 RGO:14460 miliary lung opacities in a neonate or young infant RGO:14460 ICD10CM:J21 SNOMEDCT:5505005 RGO:14461 acute bronchiolitis RGO:14461 RGO:14464 widespread small irregular lung opacities RGO:14464 ORDO:31837 SNOMEDCT:89420002 RGO:14485 pulmonary veno-occlusive disease RGO:14485 DOID:849 SNOMEDCT:398726004 RGO:14486 rheumatoid lung disease RGO:14486 RGO:14487 small airways disease RGO:14487 RGO:14491 interstitial lung fibrosis RGO:14491 IPF UIP bronchiolar emphysema chronic interstitial pneumonitis diffuse chronic fibrosing interstitial pneumonitis diffuse interstitial fibrosis fibrosing alveolitis muscular cirrhosis organizing interstitial pneumonia sclerosing alveolitis usual interstitial pneumonitis DOID:0050156 ICD10CM:J84.112 ORDO:2032 RADLEX:RID28836 SNOMEDCT:700250006 RGO:14505 idiopathic pulmonary fibrosis RGO:14505 RGO:14517 noxious gases RGO:14517 RGO:14520 diffuse interstitial disease with pleural effusion RGO:14520 DOID:10320 ICD10CM:J61 RADLEX:RID5346 SNOMEDCT:22607003 RGO:14524 asbestosis RGO:14524 RGO:14529 diffuse interstitial lung disease with associated lymphadenopathy RGO:14529 RGO:14547 ground-glass pulmonary opacity RGO:14547 DOID:2799 HP:0011946 SNOMEDCT:40100001 RGO:14553 bronchiolitis obliterans RGO:14553 HP:0005942 ORDO:98852 SNOMEDCT:8549006 RGO:14554 desquamative interstitial pneumonitis RGO:14554 DOID:5870 ICD10CM:J82 RADLEX:RID5351 SNOMEDCT:367542003 RGO:14555 eosinophilic pneumonia RGO:14555 RGO:14557 chronic air-space consolidation RGO:14557 DOID:9502 SNOMEDCT:233692000 RGO:14558 chronic eosinophilic pneumonia RGO:14558 HP:0025177 RGO:14559 peribronchovascular interstitial thickening RGO:14559 DOID:10322 ICD10CM:J63.2 SNOMEDCT:8247009 RGO:14564 berylliosis RGO:14564 RGO:14567 increased lung lucency RGO:14567 RADLEX:RID28522 SNOMEDCT:53099003 RGO:14569 pneumatocele RGO:14569 RGO:14570 upper lung disease RGO:14570 RGO:14571 silicosis and coal-worker pneumoconiosis RGO:14571 SNOMEDCT:73144008 RGO:14572 talcosis RGO:14572 RGO:14573 lower lung disease RGO:14573 RADLEX:RID5232 RGO:14575 lymphangitic carcinomatosis RGO:14575 RGO:14576 small lung nodules RGO:14576 RGO:14581 pulmonary metastases RGO:14581 RGO:14585 perilymphatic small lung nodules RGO:14585 RGO:14588 randomly distributed small lung nodules RGO:14588 RGO:14589 centrilobular small lung nodules RGO:14589 DOID:2942 HP:0011950 RADLEX:RID28499 SNOMEDCT:4120002 RGO:14590 bronchiolitis RGO:14590 DOID:1324 RGO:14592 lung neoplasm RGO:14592 DOID:2615 HP:0012740 RADLEX:RID4275 SNOMEDCT:23730008 SNOMEDCT:711329002 RGO:14593 papilloma RGO:14593 RADLEX:RID3859 SNOMEDCT:35073002 RGO:14603 inflammatory pseudotumor RGO:14603 RGO:14604 lymphoproliferative lesion RGO:14604 RADLEX:RID4282 SNOMEDCT:72938002 RGO:14605 tumorlet RGO:14605 RGO:14606 pediatric chest tumor RGO:14606 PNET of the chest wall DOID:0050608 SNOMEDCT:128783001 RGO:14609 Askin tumor RGO:14609 DOID:4765 ORDO:64741 RADLEX:RID4546 SNOMEDCT:189815007 SNOMEDCT:43149009 RGO:14612 pulmonary blastoma RGO:14612 lung lesion smaller than 4 cm ICD10CM:R91.1 RADLEX:RID35095 SNOMEDCT:427359005 RGO:14616 solitary pulmonary nodule RGO:14616 RGO:14622 round pneumonia RGO:14622 SNOMEDCT:67103005 RGO:14631 gumma RGO:14631 RGO:14640 pulmonary plasmacytoma RGO:14640 ICD10CM:M06.3 RADLEX:RID3878 SNOMEDCT:33719002 SNOMEDCT:50782009 RGO:14644 rheumatoid nodule RGO:14644 RGO:14646 solitary pulmonary mass RGO:14646 RGO:14658 hematoma of lung RGO:14658 RGO:14683 mass-like perihilar opacity RGO:14683 RGO:14690 shaggy lung nodule RGO:14690 SNOMEDCT:63130001 RGO:14699 postoperative scar RGO:14699 RGO:14700 radiation-treated carcinoma RGO:14700 SNOMEDCT:445249002 RGO:14702 multiple pulmonary nodules RGO:14702 RGO:14711 hematomas of lung RGO:14711 RGO:14712 hydatid cysts RGO:14712 RGO:14718 papillomatosis of lung RGO:14718 RGO:14721 pulmonary infarcts RGO:14721 RGO:14723 thin-walled lung cavity RGO:14723 RGO:14732 cystic adenomatoid malformation RGO:14732 SNOMEDCT:72237000 RGO:14741 septic embolus RGO:14741 RGO:14743 thick-walled lung cavity RGO:14743 RGO:14751 cavitary lung lesion in an infant or child RGO:14751 RGO:14768 rheumatoid nodules with cavitation RGO:14768 bronchial cartilage deficiency SNOMEDCT:233788001 RGO:14771 Williams-Campbell syndrome RGO:14771 RGO:14772 solitary sharply-outlined cavitary lung lesion RGO:14772 RGO:14779 solitary irregular cavitary lung lesion RGO:14779 KS DOID:8632 ORDO:33276 RADLEX:RID3999 SNOMEDCT:109385007 RGO:14784 Kaposi sarcoma RGO:14784 pulmonary abscess DOID:0060317 HP:0025044 RGO:14788 lung abscess RGO:14788 RGO:14792 debilitation RGO:14792 DOID:3087 HP:0000230 SNOMEDCT:66383009 RGO:14796 gingivitis RGO:14796 DOID:10456 HP:0011110 RADLEX:RID3674 SNOMEDCT:90176007 RGO:14797 tonsillitis RGO:14797 RGO:14801 peptic disease RGO:14801 RGO:14810 hemorrhage in lung with interstitial emphysema RGO:14810 RGO:14811 hydrocarbon aspiration RGO:14811 RGO:14814 multiple cavitary lung lesions RGO:14814 RGO:14821 pneumatoceles RGO:14821 RGO:14827 granulomas RGO:14827 RGO:14830 rheumatoid nodules RGO:14830 destructive lung opacity RGO:14833 extensive pulmonary opacity with cavitation RGO:14833 RGO:14839 traumatic laceration of lung RGO:14839 bullseye sign meniscus sign RGO:14842 mass in a pulmonary cavity RGO:14842 RGO:14843 abscess with inspissated pus RGO:14843 RGO:14849 bilateral hyperinflated lungs RGO:14849 INH SNOMEDCT:387472004 SNOMEDCT:81335000 RGO:14875 isoniazid RGO:14875 lobar air trapping neonatal lobar hyperinflation ORDO:1928 SNOMEDCT:66987001 RGO:14880 congenital lobar emphysema RGO:14880 ICD10CM:T17.5 SNOMEDCT:282461001 RGO:14885 foreign body in bronchus RGO:14885 SNOMEDCT:126705004 RGO:14887 neoplasm of bronchus RGO:14887 RGO:14888 postinflammatory cyst RGO:14888 left pulmonary artery arising from right pulmonary artery pulmonary artery sling RADLEX:RID35466 SNOMEDCT:253638007 RGO:14889 pulmonary sling RGO:14889 HP:0002643 RGO:14890 neonatal respiratory distress RGO:14890 DOID:424 SNOMEDCT:42908004 RGO:14893 pulmonary immaturity RGO:14893 RGO:14896 eventration or paralysis of diaphragm RGO:14896 HP:0008750 RGO:14897 laryngeal atresia RGO:14897 RGO:14899 overly medicated mother RGO:14899 RGO:14902 bubbly lungs in infants and children RGO:14902 DOID:11650 ORDO:70589 SNOMEDCT:67569000 RGO:14904 bronchopulmonary dysplasia RGO:14904 Mikity-Wilson syndrome ICD10CM:P27.0 SNOMEDCT:51577008 RGO:14907 Wilson-Mikity syndrome RGO:14907 RGO:14908 bilateral pulmonary underaeration RGO:14908 RGO:14910 poor inspiration RGO:14910 RGO:14911 bilateral diaphragmatic eventration RGO:14911 RGO:14912 Cheyne-Stokes breathing in neonate RGO:14912 RGO:14916 neurologic disorder RGO:14916 RGO:14917 primary muscular disorder RGO:14917 RGO:14918 pulmonary hypoplasia in neonate RGO:14918 RGO:14919 asymmetric lung size RGO:14919 RGO:14923 eventration of hemidiaphragm RGO:14923 SNOMEDCT:277321001 RGO:14924 phrenic nerve paralysis RGO:14924 RGO:14930 lung transplantation RGO:14930 Macleod syndrome Swyer-James-McLeod syndrome unilateral hyperlucent lung syndrome ICD10CM:J43.0 SNOMEDCT:45145000 RGO:14931 Swyer-James syndrome RGO:14931 RGO:14932 thoracoplasty RGO:14932 RGO:14933 localized chronic pulmonary opacity RGO:14933 RGO:14944 unilateral diffuse lung disease RGO:14944 SNOMEDCT:77920006 RGO:14955 pulmonary gangrene RGO:14955 RGO:14957 bilateral basilar lung disease RGO:14957 viral lung disease DOID:10533 RADLEX:RID34769 SNOMEDCT:75570004 RGO:14963 viral pneumonia RGO:14963 ORDO:86869 RADLEX:RID3689 SNOMEDCT:239940004 RGO:14966 lymphomatoid granulomatosis RGO:14966 RGO:14969 retrocardiac lesion RGO:14969 RGO:14971 atelectasis of lower lobe RGO:14971 RGO:14982 indistinct heart border on frontal chest radiograph RGO:14982 RADLEX:RID1429 RGO:14986 pericardial fat pad RGO:14986 SNOMEDCT:2778004 RGO:14987 pleural fluid RGO:14987 subpleural lung lesion RGO:14993 peripheral lung lesion RGO:14993 RGO:15001 long linear lung shadow RGO:15001 RGO:15012 mucoid impaction in bronchus RGO:15012 HHT Rendu-Osler-Weber syndrome familial telangiectasia hereditary hemorrhagic telangiectasia RGO:15024 Osler-Weber-Rendu syndrome RGO:15024 DOID:3482 ICD10CM:A20 ORDO:707 SNOMEDCT:58750007 RGO:15026 plague RGO:15026 DOID:0050468 ICD10CM:L60.5 ORDO:662 SNOMEDCT:400211001 RGO:15027 yellow nail syndrome RGO:15027 RGO:15042 lung disease with eosinophilia RGO:15042 DOID:999 ORDO:168956 SNOMEDCT:128835008 SNOMEDCT:423294001 RGO:15053 hypereosinophilic syndrome RGO:15053 EAA extrinsic allergic alveolitis organic dust disease HP:0006516 ORDO:31740 SNOMEDCT:37471005 RGO:15054 hypersensitivity pneumonitis RGO:15054 DOID:14453 ORDO:99906 RGO:15057 farmer lung RGO:15057 RGO:15061 basement shower extrinsic allergic alveolitis RGO:15061 RGO:15062 black fat tobacco disease RGO:15062 RGO:15063 building-associated extrinsic allergic alveolitis RGO:15063 RGO:15064 castor bean lung RGO:15064 RGO:15065 cave explorer lung RGO:15065 RGO:15066 cheese brusher lung RGO:15066 RGO:15067 coffee-worker lung RGO:15067 RGO:15068 detergent-worker lung RGO:15068 RGO:15069 fish meal-worker lung RGO:15069 RGO:15070 fog-fever RGO:15070 RGO:15071 furrier lung RGO:15071 RGO:15072 green coffee-worker disease RGO:15072 RGO:15073 hemp dust inhalation disease RGO:15073 RGO:15074 hot-tub lung RGO:15074 RGO:15075 isocyanate-associated extrinsic allergic alveolitis RGO:15075 RGO:15076 Japanese summer-type extrinsic allergic alveolitis RGO:15076 RGO:15077 malt worker pneumonia RGO:15077 RGO:15078 maple bark stripper disease RGO:15078 lycoperdonosis RGO:15079 mushroom-worker lung RGO:15079 RGO:15080 organophosphate insecticide inhalation RGO:15080 RGO:15081 paprika splitter lung RGO:15081 RGO:15082 pituitary snuff-taker lung RGO:15082 RGO:15083 prawn-worker lung RGO:15083 ICD10CM:J67.8 SNOMEDCT:23315001 RGO:15084 sequoiosis RGO:15084 RGO:15085 starch sprayer lung RGO:15085 RGO:15087 thatched roof dust disease RGO:15087 SNOMEDCT:38729007 RGO:15089 wheat weevil disease RGO:15089 RGO:15090 wood pulp-worker lung RGO:15090 DOID:10316 RADLEX:RID5343 SNOMEDCT:40122008 RGO:15091 pneumoconiosis RGO:15091 RGO:15092 asbestos inhalation RGO:15092 SNOMEDCT:34323004 RGO:15093 coal RGO:15093 SNOMEDCT:83581005 RGO:15094 silica RGO:15094 RGO:15096 antimony exposure RGO:15096 RADLEX:RID11768 SNOMEDCT:88014003 RGO:15098 beryllium RGO:15098 RADLEX:RID11856 SNOMEDCT:66586000 RGO:15099 cadmium RGO:15099 RGO:15101 cement dust RGO:15101 SNOMEDCT:33817009 RGO:15104 diatomaceous earth RGO:15104 SNOMEDCT:68329003 RGO:15105 fuller earth RGO:15105 SNOMEDCT:8865003 RGO:15106 graphite RGO:15106 RGO:15109 manganese inhalation RGO:15109 SNOMEDCT:24605005 RGO:15110 mica RGO:15110 RADLEX:RID11912 SNOMEDCT:72578004 RGO:15111 osmium RGO:15111 RGO:15112 platinum inhalation RGO:15112 SNOMEDCT:256518006 SNOMEDCT:35233000 RGO:15113 polyvinyl chloride RGO:15113 SNOMEDCT:14132003 RGO:15114 silicon carbide RGO:15114 RGO:15116 synthetic mineral fibers RGO:15116 RADLEX:RID11806 SNOMEDCT:18925001 RGO:15120 vanadium RGO:15120 RGO:15121 volcanic dust inhalation RGO:15121 RGO:15123 zirconium inhalation RGO:15123 RGO:15125 vapor-induced lung disease RGO:15125 RADLEX:RID11830 SNOMEDCT:85378003 RGO:15127 bromine RGO:15127 RADLEX:RID11794 SNOMEDCT:29276003 RGO:15128 chlorine RGO:15128 SNOMEDCT:255644009 RGO:15130 carbon tetrachloride RGO:15130 SNOMEDCT:65773003 RGO:15131 chloropicrin RGO:15131 SNOMEDCT:259133007 RGO:15132 methyl bromide RGO:15132 SNOMEDCT:88381009 RGO:15133 methyl chloride RGO:15133 SNOMEDCT:16808006 RGO:15134 trichloroethylene RGO:15134 SNOMEDCT:421024009 SNOMEDCT:43953005 RGO:15139 ammonia RGO:15139 SNOMEDCT:42757007 RGO:15140 hydrogen fluoride RGO:15140 SNOMEDCT:27390006 RGO:15141 hydrogen sulfide RGO:15141 SNOMEDCT:74981003 RGO:15142 lewisite RGO:15142 SNOMEDCT:76533004 RGO:15143 mustard gas RGO:15143 SNOMEDCT:21888005 RGO:15144 nickel carbonyl RGO:15144 RGO:15145 phosgene gas inhalation RGO:15145 SNOMEDCT:86233005 RGO:15146 sulfur dioxide RGO:15146 SNOMEDCT:333511003 SNOMEDCT:4370008 RGO:15147 acetone RGO:15147 SNOMEDCT:85937005 RGO:15148 acrolein RGO:15148 RGO:15150 insecticides RGO:15150 SNOMEDCT:77793008 RGO:15151 isoamyl acetate RGO:15151 SNOMEDCT:40057008 RGO:15153 ozone RGO:15153 SNOMEDCT:64197008 RGO:15154 smoke RGO:15154 RGO:15155 chemical-induced lung disease RGO:15155 SNOMEDCT:31087008 SNOMEDCT:387170002 RGO:15156 ampicillin RGO:15156 RGO:15157 cephalosporin RGO:15157 SNOMEDCT:24450004 SNOMEDCT:387129004 RGO:15158 ethambutol RGO:15158 SNOMEDCT:372807004 SNOMEDCT:64349004 RGO:15159 griseofulvin RGO:15159 SNOMEDCT:373543005 SNOMEDCT:85343003 RGO:15161 nitrofurantoin RGO:15161 PAS SNOMEDCT:255666002 SNOMEDCT:27192005 RGO:15162 para-aminosalicylic acid RGO:15162 SNOMEDCT:373270004 SNOMEDCT:6369005 RGO:15163 penicillin RGO:15163 SNOMEDCT:373769001 SNOMEDCT:59589008 RGO:15164 pyrimethamine RGO:15164 SNOMEDCT:387406002 SNOMEDCT:59255006 RGO:15165 sulfonamide RGO:15165 5FU RGO:15167 5-fluoruracil RGO:15167 RGO:15168 6-mercaptopuran RGO:15168 SNOMEDCT:111165009 SNOMEDCT:372574004 RGO:15169 azathioprine RGO:15169 SNOMEDCT:372843005 SNOMEDCT:76591000 RGO:15170 bleomycin RGO:15170 SNOMEDCT:2571007 SNOMEDCT:387138002 RGO:15171 busulfan RGO:15171 SNOMEDCT:387249003 SNOMEDCT:46009007 RGO:15172 chlorambucil RGO:15172 SNOMEDCT:387467008 SNOMEDCT:80906007 RGO:15174 cyclosporin A RGO:15174 SNOMEDCT:387511003 SNOMEDCT:89265009 RGO:15175 cytosine arabinoside RGO:15175 SNOMEDCT:387316009 SNOMEDCT:56928005 RGO:15176 etoposide RGO:15176 SNOMEDCT:108763009 SNOMEDCT:386907005 RGO:15177 fludarabine RGO:15177 SNOMEDCT:387314007 SNOMEDCT:56602009 RGO:15179 hydroxyurea RGO:15179 RGO:15180 ifosphamide RGO:15180 SNOMEDCT:38476002 RGO:15181 interleukin RGO:15181 SNOMEDCT:371014004 RGO:15182 L-asparaginase RGO:15182 SNOMEDCT:387297002 SNOMEDCT:544002 RGO:15183 melphalan RGO:15183 ORDO:90070 SNOMEDCT:387381009 SNOMEDCT:68887009 RGO:15184 methotrexate RGO:15184 SNOMEDCT:387331000 SNOMEDCT:59240002 RGO:15185 mitomycin RGO:15185 RGO:15186 nitrosoureas RGO:15186 RGO:15187 peplomycin RGO:15187 SNOMEDCT:387474003 SNOMEDCT:81583003 RGO:15188 procarbazine RGO:15188 SNOMEDCT:61864009 RGO:15189 vinca alkaloid RGO:15189 SNOMEDCT:387458008 SNOMEDCT:7947003 RGO:15191 acetylsalicylic acid RGO:15191 SNOMEDCT:387494007 SNOMEDCT:85990009 RGO:15192 codeine RGO:15192 ORDO:31824 SNOMEDCT:387413002 SNOMEDCT:73133000 RGO:15193 colchicine RGO:15193 SNOMEDCT:387501005 SNOMEDCT:86977007 RGO:15194 mesalamine RGO:15194 RGO:15196 bromocarbamide RGO:15196 SNOMEDCT:31684002 SNOMEDCT:387173000 RGO:15197 buprenorphine RGO:15197 Librium SNOMEDCT:372866006 SNOMEDCT:82746003 RGO:15198 chlordiazepoxide RGO:15198 Placidyl SNOMEDCT:111126006 SNOMEDCT:400660004 RGO:15199 ethchlorvynol RGO:15199 RGO:15200 febarbamate RGO:15200 SNOMEDCT:387341002 SNOMEDCT:60881009 RGO:15201 heroin RGO:15201 SNOMEDCT:387286002 SNOMEDCT:51758009 RGO:15202 methadone RGO:15202 SNOMEDCT:372890007 SNOMEDCT:89018006 RGO:15203 naloxone RGO:15203 Darvon SNOMEDCT:117005003 SNOMEDCT:387042001 RGO:15204 propoxyphene RGO:15204 SNOMEDCT:387222003 SNOMEDCT:40820003 RGO:15206 carbamazepine RGO:15206 SNOMEDCT:386170005 SNOMEDCT:70732003 RGO:15208 trimethadione RGO:15208 RGO:15210 coumadin RGO:15210 SNOMEDCT:372756006 SNOMEDCT:48603004 RGO:15211 warfarin RGO:15211 RGO:15215 5-aminosalycilic acid RGO:15215 SNOMEDCT:372821002 SNOMEDCT:69236009 RGO:15216 amiodarone RGO:15216 SNOMEDCT:372726002 SNOMEDCT:40589005 RGO:15217 amitriptyline RGO:15217 RGO:15218 beclomethasone diproprionate aerosol RGO:15218 beta-blocker SNOMEDCT:33252009 RGO:15219 beta-adrenergic blocking agent RGO:15219 RGO:15220 beta-2 sympathomimetic with corticosteroid RGO:15220 SNOMEDCT:111154004 SNOMEDCT:386991003 RGO:15222 chlorpropamide RGO:15222 SNOMEDCT:372903001 SNOMEDCT:96209002 RGO:15223 clomipramine RGO:15223 DOID:809 ICD10CM:F14.1 ORDO:90068 SNOMEDCT:78267003 RGO:15224 cocaine abuse RGO:15224 RGO:15225 desferioxamine RGO:15225 RGO:15226 diproprionate aerosol RGO:15226 Prozac SNOMEDCT:75115009 RGO:15228 fluoxetine hydrochloride RGO:15228 SNOMEDCT:36113004 SNOMEDCT:372718005 RGO:15229 imipramine RGO:15229 RADLEX:RID49907 SNOMEDCT:387480006 SNOMEDCT:82573000 RGO:15230 lidocaine RGO:15230 SNOMEDCT:10083006 SNOMEDCT:398705004 RGO:15231 marijuana RGO:15231 SNOMEDCT:272165008 RGO:15232 methacrylate RGO:15232 Sansert SNOMEDCT:11796006 SNOMEDCT:387044000 RGO:15233 methysergide RGO:15233 SNOMEDCT:111089004 SNOMEDCT:354035004 RGO:15234 mineral oil RGO:15234 RGO:15235 neocarzinostatin RGO:15235 SNOMEDCT:387235007 SNOMEDCT:4219002 RGO:15236 penicillamine RGO:15236 SNOMEDCT:372839006 RGO:15237 phenothiazine RGO:15237 Pronestyl SNOMEDCT:11959009 SNOMEDCT:372589008 RGO:15238 procainamide RGO:15238 SNOMEDCT:3814009 SNOMEDCT:387203007 RGO:15239 propylthiouracil RGO:15239 SNOMEDCT:387248006 SNOMEDCT:45844004 RGO:15240 sulfasalazine RGO:15240 SNOMEDCT:10555000 SNOMEDCT:372479006 RGO:15242 tocainide RGO:15242 SNOMEDCT:373550009 SNOMEDCT:90426002 RGO:15243 trimipramine RGO:15243 SNOMEDCT:372754009 SNOMEDCT:47898004 RGO:15244 verapamil RGO:15244 RGO:15245 infectious lung disease RGO:15245 RGO:15248 adenovirus RGO:15248 RGO:15249 Aerobacter infection RGO:15249 RGO:15250 Aeromonas infection RGO:15250 RGO:15251 Bacteroides infection RGO:15251 RGO:15252 Brucella infection RGO:15252 RGO:15253 Clostridium infection RGO:15253 RGO:15255 ECHO viruses RGO:15255 RGO:15256 Enterobacter-Serratia infection RGO:15256 SNOMEDCT:40168006 RGO:15257 Epstein-Barr virus RGO:15257 RGO:15258 Eubacterium infection RGO:15258 hantavirosis hantavirus infection RGO:15259 hanta virus infection RGO:15259 RGO:15260 influenza viruses RGO:15260 SNOMEDCT:26726000 RGO:15261 Legionella infection RGO:15261 RGO:15262 leptospira organisms RGO:15262 SNOMEDCT:312105006 RGO:15263 Morganella infection RGO:15263 RGO:15264 parainfluenza virus RGO:15264 SNOMEDCT:50517009 RGO:15266 Proteus species RGO:15266 SNOMEDCT:6415009 RGO:15267 respiratory syncytial virus RGO:15267 SNOMEDCT:52584002 RGO:15268 rubeola virus RGO:15268 SNOMEDCT:27268008 RGO:15269 Salmonella species RGO:15269 RGO:15270 Viellonella species RGO:15270 RGO:15271 Armillifer infection RGO:15271 RGO:15272 Babesia infection RGO:15272 RGO:15274 Filaria infection RGO:15274 RGO:15275 Hartmanella-Acanthamoeba infection RGO:15275 RGO:15276 Microsporidia infection RGO:15276 RGO:15280 Aspergillus infection RGO:15280 RGO:15282 Geotrichum infection RGO:15282 RGO:15284 opportunistic lung infection RGO:15284 SNOMEDCT:44247006 RGO:15297 prematurity RGO:15297 RGO:15300 pulmonary disease in an immunodeficient patient RGO:15300 RGO:15301 drug-induced lung disease RGO:15301 RGO:15308 lymphangiography reaction RGO:15308 NSIP nonspecific interstitial pneumonia RGO:15309 nonspecific interstitial pneumonitis RGO:15309 DOID:14557 HP:0002092 ICD10CM:I27.0 RGO:15310 primary pulmonary hypertension RGO:15310 RGO:15312 bronchial lesion RGO:15312 RADLEX:RID28501 SNOMEDCT:69921001 RGO:15314 broncholith RGO:15314 ICD10CM:J86.0 SNOMEDCT:233793003 RGO:15320 bronchopleural fistula RGO:15320 RGO:15322 fracture or laceration of bronchus RGO:15322 SNOMEDCT:76914003 RGO:15328 tracheal bronchus RGO:15328 SNOMEDCT:54675009 RGO:15329 tracheopathia osteoplastica RGO:15329 bronchial mucoid impaction mucoid impaction in a bronchus SNOMEDCT:6078006 RGO:15330 mucoid impaction RGO:15330 HP:0030715 SNOMEDCT:50513008 RGO:15335 bronchial atresia RGO:15335 RGO:15336 bronchial cyst RGO:15336 RGO:15338 chronic aspiration RGO:15338 ORDO:3471 SNOMEDCT:233666007 RGO:15349 Young syndrome RGO:15349 RADLEX:RID28497 SNOMEDCT:29424000 RGO:15351 bronchiolectasis RGO:15351 RGO:15358 intratracheal mass RGO:15358 RGO:15365 ectopic endotracheal thymus RGO:15365 RGO:15373 storage diseases RGO:15373 RGO:15377 pedunculated intratracheal mass RGO:15377 RGO:15379 inspissated mucus RGO:15379 RGO:15382 postintubation tracheal granuloma in neonate RGO:15382 enlarged trachea tracheal enlargement RGO:15383 large trachea RGO:15383 HP:0004313 SNOMEDCT:417167007 RGO:15385 immunoglobulin deficiency RGO:15385 SNOMEDCT:33094002 RGO:15386 tracheocele RGO:15386 RGO:15387 diffuse tracheal narrowing RGO:15387 laryngotracheobronchitis DOID:9395 RADLEX:RID3400 SNOMEDCT:71186008 RGO:15388 croup RGO:15388 DOID:4424 ORDO:158000 RADLEX:RID3854 SNOMEDCT:400031009 RGO:15397 juvenile xanthogranuloma RGO:15397 displacement of trachea RGO:15404 tracheal displacement RGO:15404 widening of right tracheal stripe RGO:15414 wide right tracheal stripe RGO:15414 RGO:15428 superior mediastinal mass RGO:15428 RADLEX:RID1588 RGO:15433 esophageal dilatation RGO:15433 RGO:15440 anomalous left superior vena cava RGO:15440 RGO:15445 parathyroid adenoma or carcinoma RGO:15445 RGO:15446 wide superior mediastinum in an infant or child RGO:15446 RGO:15459 anterior mediastinal lesion RGO:15459 RADLEX:RID3280 RGO:15470 pericardial disease RGO:15470 RGO:15471 superior vena cava dilatation RGO:15471 middle mediastinal mass RGO:15481 middle mediastinal lesion RGO:15481 HP:0004927 SNOMEDCT:93059006 RGO:15490 pulmonary artery dilatation RGO:15490 DOID:3277 RGO:15500 thymic neoplasm RGO:15500 RGO:15503 posterior mediastinal lesion RGO:15503 RGO:15513 mediastinal varices RGO:15513 RGO:15524 fat-attenuation mediastinal mass RGO:15524 DOID:1975 SNOMEDCT:447137005 RGO:15529 thymolipoma RGO:15529 RGO:15530 water-attenuation mediastinal lesion RGO:15530 SNOMEDCT:1198000100000410 RGO:15534 paraspinal abscess RGO:15534 RGO:15535 esophagectomy with gastric or colon interposition RGO:15535 RGO:15538 soft-tissue mediastinal mass RGO:15538 RGO:15552 spindle cell tumor RGO:15552 RGO:15553 calcified mediastinal mass RGO:15553 RGO:15562 enhancing mediastinal mass RGO:15562 SNOMEDCT:254646001 RGO:15567 localized fibrous tumor of pleura RGO:15567 RGO:15571 vascular abnormality of mediastinum RGO:15571 RGO:15575 high aortic arch RGO:15575 RGO:15576 right anterior aortic arch with mirror-image branching RGO:15576 RGO:15584 circumflex right aortic arch with left descending aorta RGO:15584 RGO:15586 left aortic arch with aberrant right subclavian artery RGO:15586 SNOMEDCT:9642004 RGO:15589 left superior vena cava RGO:15589 RGO:15590 pseudocoarctation of aortic arch RGO:15590 RGO:15591 right posterior aortic arch with aberrant left subclavian artery RGO:15591 RGO:15592 cystic mediastinal mass RGO:15592 RGO:15596 idiopathic mediastinal cyst RGO:15596 retrosternal goiter SNOMEDCT:66392007 RGO:15599 intrathoracic goiter RGO:15599 RGO:15603 retrosternal mass RGO:15603 RGO:15611 pleural fluid loculation RGO:15611 RGO:15619 thymic enlargement RGO:15619 DOID:2994 RADLEX:RID4314 SNOMEDCT:115233005 SNOMEDCT:402878003 RGO:15625 germ cell neoplasm RGO:15625 RGO:15626 thymic carcinoid RGO:15626 DOID:3284 ORDO:99868 SNOMEDCT:128717008 RGO:15627 thymic carcinoma RGO:15627 RADLEX:RID3942 RGO:15628 thymic cyst RGO:15628 RGO:15629 small thymus in an infant RGO:15629 RGO:15635 thymic agenesis RGO:15635 RGO:15636 right anterior cardiophrenic angle lesion RGO:15636 RGO:15637 epicardial fat pad RGO:15637 RGO:15654 abnormal azygoesophageal recess RGO:15654 RGO:15656 descending aorta dilatation RGO:15656 RGO:15660 pleural effusion or thickening RGO:15660 RGO:15663 displacement of the thoracic paraspinal line RGO:15663 RGO:15669 posterior mediastinal mass RGO:15669 RGO:15677 intrathoracic extramedullary hematopoiesis RGO:15677 SNOMEDCT:12770006 RGO:15680 cyanotic congenital heart disease RGO:15680 DOID:11758 HP:0001891 ICD10CM:D50 SNOMEDCT:87522002 RGO:15682 iron deficiency anemia RGO:15682 SNOMEDCT:302873008 RGO:15683 thrombocytopenic purpura RGO:15683 thrombocythemia DOID:2228 HP:0001894 SNOMEDCT:6631009 RGO:15684 thrombocytosis RGO:15684 RGO:15685 wide mediastinum RGO:15685 RGO:15696 allergic edema of mediastinum RGO:15696 RGO:15701 acute diffuse mediastinal widening RGO:15701 dissection of aorta HP:0002647 RADLEX:RID3320 RGO:15705 aortic dissection RGO:15705 RGO:15709 postthoracotomy lymphocele RGO:15709 RGO:15712 esophageal perforation RGO:15712 ICD10CM:A22 SNOMEDCT:409498004 RGO:15718 anthrax RGO:15718 RGO:15734 mediastinal and/or hilar lymph node enlargement RGO:15734 DOID:1016 SNOMEDCT:63309002 RGO:15742 primary tuberculosis RGO:15742 HP:0012219 ICD10CM:L52 SNOMEDCT:32861005 RGO:15746 erythema nodosum RGO:15746 RGO:15752 recurrent childhood pneumonia RGO:15752 Destombes-Rosaï-Dorfman disease Rosaï-Dorfman disease Rosaï-Dorfman-Destombes disease SHML sinus histiocytosis with massive lymphadenopathy SNOMEDCT:23041001 RGO:15753 sinus histiocytosis RGO:15753 RGO:15755 marked hilar lymphadenopathy RGO:15755 RGO:15759 bilateral hilar enlargement RGO:15759 hilar adenopathy SNOMEDCT:87500009 RGO:15761 hilar lymphadenopathy RGO:15761 RGO:15764 unilateral hilar enlargement RGO:15764 RGO:15767 infectious hilar lymphadenopathy RGO:15767 SNOMEDCT:398078006 RGO:15776 pericardial defect RGO:15776 RGO:15778 main pulmonary artery thromboembolus RGO:15778 RGO:15780 unilateral small hilar shadow RGO:15780 RGO:15782 unilateral lung hyperaeration RGO:15782 RGO:15791 hilar displacement RGO:15791 HP:0100750 ICD10CM:J98.11 RADLEX:RID28493 SNOMEDCT:46621007 RGO:15792 atelectasis RGO:15792 SNOMEDCT:173171007 RGO:15793 pulmonary lobectomy RGO:15793 RGO:15797 lobar agenesis RGO:15797 RGO:15798 lobar torsion RGO:15798 ICD10CM:R93.8 SNOMEDCT:19616004 RGO:15800 mediastinal shift RGO:15800 RGO:15825 bronchial dehiscence after lung transplant RGO:15825 RGO:15831 high altitude exercise RGO:15831 SNOMEDCT:386216000 RGO:15833 parturition RGO:15833 SNOMEDCT:441536000 RGO:15841 iatrogenic pneumothorax RGO:15841 DOID:3798 RADLEX:RID3714 SNOMEDCT:312682007 SNOMEDCT:66696003 RGO:15859 empyema RGO:15859 RGO:15868 pleural effusion with normal lungs RGO:15868 RADLEX:RID43269 RGO:15870 asbestos-related pleural disease RGO:15870 RGO:15893 pleural effusion with disease in thorax RGO:15893 DOID:3049 SNOMEDCT:82275008 RGO:15903 Churg-Strauss syndrome RGO:15903 postmyocardial infarction syndrome DOID:10507 RADLEX:RID3297 RGO:15904 Dressler syndrome RGO:15904 RGO:15911 pulmonary lymphangiomatosis RGO:15911 RGO:15913 small pleural effusion with subsegmental atelectasis RGO:15913 RGO:15917 pleural effusion with enlarged heart RGO:15917 RGO:15922 pleural effusion with disease in abdomen RGO:15922 DOID:5425 ORDO:64739 SNOMEDCT:129635004 RGO:15931 ovarian hyperstimulation syndrome RGO:15931 eosinophilic pleural effusion RGO:15932 pleural effusion containing eosinophiles RGO:15932 HP:0011920 RGO:15941 transudative pleural effusion RGO:15941 ICD10CM:E87.7 SNOMEDCT:21639008 RGO:15942 fluid overload RGO:15942 HP:0011921 SNOMEDCT:13841000119107 RGO:15945 exudative pleural effusion RGO:15945 ORDO:314451 SNOMEDCT:63402005 RGO:15950 Meigs syndrome RGO:15950 HP:0012151 ICD10CM:J94.2 RADLEX:RID34595 SNOMEDCT:31892009 RGO:15952 hemothorax RGO:15952 DOID:7683 HP:0002622 RADLEX:RID34793 RGO:15958 dissecting aortic aneurysm RGO:15958 RGO:15959 pleural adhesion tear RGO:15959 lymphothorax HP:0010310 SNOMEDCT:83035003 RGO:15960 chylothorax RGO:15960 RGO:15964 trauma to thoracic duct RGO:15964 SNOMEDCT:7377003 RGO:15967 fibrosing mediastinitis RGO:15967 RGO:15972 massive pleural effusion RGO:15972 RGO:15983 radiopaque hemithorax RGO:15983 RGO:15984 atelectasis of one lung RGO:15984 unilateral pulmonary agenesis RGO:15990 agenesis of one lung RGO:15990 ICD10CM:Q79.1 RGO:15994 eventration of diaphragm RGO:15994 RGO:15995 fibrosis of lung or pleura RGO:15995 SNOMEDCT:73725006 RGO:15999 pleural thickening RGO:15999 RGO:16009 invasive thymoma with pleural involvement RGO:16009 RGO:16012 subpleural collaterals in pulmonary venous or arterial atresia RGO:16012 tumor-like pleural thickening RGO:16013 nodular pleural thickening RGO:16013 RGO:16016 invasive thymoma with pleural involvement RGO:16016 SNOMEDCT:32931001 RGO:16017 pleural calcification RGO:16017 SNOMEDCT:6480001000004101 RGO:16030 pleural mass RGO:16030 RGO:16039 fibrin ball RGO:16039 RGO:16041 multiple pleural masses RGO:16041 RGO:16045 invasive thymoma RGO:16045 RGO:16049 chest wall lesion RGO:16049 RGO:16066 pleural-based lesion RGO:16066 RGO:16069 axillary mass RGO:16069 RGO:16071 empyema necessitatis RGO:16071 RGO:16074 pediatric chest wall lesion RGO:16074 RADLEX:RID4291 SNOMEDCT:47284001 RGO:16079 desmoid RGO:16079 DOID:4769 HP:0100528 ORDO:64742 SNOMEDCT:128763002 SNOMEDCT:707670009 RGO:16081 pleuropulmonary blastoma RGO:16081 RGO:16084 short narrow thoracic cage RGO:16084 RGO:16089 Barnes syndrome RGO:16089 RGO:16091 chest malformation RGO:16091 HP:0002089 RGO:16098 pulmonary hypoplasia RGO:16098 RADLEX:RID28525 SNOMEDCT:233645004 RGO:16103 tension pneumothorax RGO:16103 RGO:16107 hyperaeration with acidosis and dehydration RGO:16107 RGO:16111 bilateral elevated diaphragm RGO:16111 RGO:16114 expiratory or poor inspiratory film RGO:16114 RGO:16115 hepatomegaly and splenomegaly RGO:16115 RGO:16118 bilateral eventration RGO:16118 RGO:16120 bilateral lobar atelectasis RGO:16120 RGO:16122 bilateral pleural disease RGO:16122 RGO:16124 bilateral subphrenic abscess RGO:16124 elevated hemidiaphragm RGO:16125 unilaterally elevated diaphragm RGO:16125 RADLEX:RID5248 SNOMEDCT:37291000 RGO:16127 eventration RGO:16127 RGO:16147 traumatic diaphragmatic rupture RGO:16147 fixed hemidiaphragm RGO:16148 paralyzed hemidiaphragm RGO:16148 RGO:16157 phrenic nerve paralysis or dysfunction RGO:16157 diaphragmatic scalloping mogul of diaphragm scalloping of diaphragm scalloping of hemidiaphragm RGO:16164 localized elevation of hemidiaphragm RGO:16164 RGO:16176 segmental paralysis of phrenic nerve RGO:16176 RGO:16177 juxtadiaphragmatic lesions in children RGO:16177 RGO:16184 solitary thoracic calcification RGO:16184 RGO:16194 bronchogenic carcinoma engulfing a granuloma RGO:16194 RGO:16205 multifocal thoracic calcification RGO:16205 RGO:16216 lymphoma after radiation therapy RGO:16216 RGO:16222 calcified pulmonary metastasis RGO:16222 psammomatous adenocarcinoma DOID:3112 SNOMEDCT:4797003 RGO:16224 papillary adenocarcinoma RGO:16224 RGO:16228 eggshell calcification in the chest RGO:16228 RGO:16229 aneurysm of great vessels RGO:16229 RGO:16234 congenital renal or ureteral anomaly RGO:16234 Potter syndrome oligohydramnios sequence DOID:12594 RGO:16235 Potter sequence RGO:16235 ORDO:557 SNOMEDCT:33225004 RGO:16236 anorectal malformation RGO:16236 BOR syndrome Melnick-Fraser syndrome DOID:14702 SNOMEDCT:290006 RGO:16238 branchio-oto-renal syndrome RGO:16238 RGO:16240 craniosynostosis syndromes RGO:16240 RGO:16241 Dietl syndrome RGO:16241 DOID:3614 ORDO:478 RGO:16242 Kallmann syndrome RGO:16242 DOID:0060259 ORDO:294415 RGO:16245 renal-hepatic-pancreatic dysplasia RGO:16245 mermaid syndrome sympus apus HP:0010497 ORDO:3169 SNOMEDCT:67254002 RGO:16246 sirenomelia RGO:16246 renal insufficiency DOID:557 HP:0000112 ICD10CM:N08 RADLEX:RID5304 SNOMEDCT:90708001 RGO:16247 nephropathy RGO:16247 RGO:16251 polycystic kidneys and liver RGO:16251 RGO:16256 familial hyperuricosuria RGO:16256 FJN NPHP autosomal recessive medullary cystic kidney disease familial juvenile nephronophthisis juvenile nephronophthisis DOID:12712 HP:0000090 SNOMEDCT:204958008 RGO:16258 nephronophthisis RGO:16258 DOID:0050576 ORDO:3156 RGO:16260 Senior-Loken syndrome RGO:16260 malpositioned kidney RGO:16261 malposition of kidney RGO:16261 renal ectopia HP:0000086 ICD10CM:Q63.2 RADLEX:RID34714 SNOMEDCT:16507009 RGO:16263 ectopic kidney RGO:16263 HP:0002566 RADLEX:RID4812 RGO:16266 malrotation RGO:16266 RGO:16271 psoas muscle hypertrophy RGO:16271 RGO:16273 mass displacing kidney RGO:16273 RGO:16282 unilateral absence or blurring of renal outline RGO:16282 RGO:16284 congenital absence or aplasia of kidney RGO:16284 HP:0000086 RGO:16285 displaced kidney RGO:16285 RGO:16288 atrophic kidney RGO:16288 RGO:16291 decreased size of part of a kidney RGO:16291 RGO:16296 traumatic renal atrophy RGO:16296 DOID:1063 HP:0001970 RADLEX:RID5312 SNOMEDCT:264536006 SNOMEDCT:28689008 RGO:16298 interstitial nephritis RGO:16298 SNOMEDCT:7185004 RGO:16301 unilateral small kidney RGO:16301 RGO:16306 posttraumatic atrophy RGO:16306 SNOMEDCT:7725007 RGO:16310 radiation nephritis RGO:16310 SNOMEDCT:52777008 RGO:16316 bilateral small kidneys RGO:16316 RGO:16321 reflux atrophy RGO:16321 RGO:16325 congenital renal hypoplasia RGO:16325 DOID:581 SNOMEDCT:190829000 RGO:16329 gouty nephropathy RGO:16329 RGO:16334 lead nephropathy RGO:16334 RGO:16336 late papillary necrosis RGO:16336 RGO:16338 postobstructive atrophy RGO:16338 RGO:16341 unilateral large kidney RGO:16341 RGO:16345 double or triple collecting system RGO:16345 RGO:16351 congenital megacalyces RGO:16351 Perlman tumor cystic nephroma mixed epithelial stromal tumor renal epithelial stromal tumor RGO:16356 multilocular cystic nephroma RGO:16356 RGO:16360 bilateral large kidneys RGO:16360 DOID:2921 HP:0000099 ICD10CM:N08 SNOMEDCT:36171008 RGO:16363 glomerulonephritis RGO:16363 RGO:16364 multiple simple cysts RGO:16364 ICD10CM:N17.1 RGO:16368 acute cortical necrosis RGO:16368 ATN DOID:12556 HP:0008682 ICD10CM:N17.0 RADLEX:RID5311 SNOMEDCT:35455006 RGO:16370 acute tubular necrosis RGO:16370 DOID:1311 RGO:16371 AIDS nephropathy RGO:16371 DOID:4971 SNOMEDCT:128843003 SNOMEDCT:52967002 RGO:16372 agnogenic myeloid metaplasia RGO:16372 RGO:16381 metastases to kidneys RGO:16381 SNOMEDCT:57414003 RGO:16390 tyrosinosis RGO:16390 RGO:16393 large kidneys with multifocal masses RGO:16393 acquired cystic kidney disease acquired polycystic kidney disease SNOMEDCT:105999006 RGO:16396 acquired renal cystic disease RGO:16396 RGO:16401 decreased nephrogram RGO:16401 ICD10CM:N28.0 SNOMEDCT:236488005 RGO:16403 renal artery occlusion RGO:16403 RGO:16404 renal vein occlusion RGO:16404 RGO:16405 contrast administration error RGO:16405 RGO:16407 focal defect in nephrogram RGO:16407 DOID:559 ICD10CM:N10 SNOMEDCT:36689008 RGO:16408 acute pyelonephritis RGO:16408 RGO:16421 dense nephrogram RGO:16421 RGO:16427 normal kidneys with rapid bolus contrast medium injection RGO:16427 RGO:16432 traumatic reflex anuria RGO:16432 RGO:16433 cortical necrosis RGO:16433 RGO:16435 lymphoma with urate nephropathy RGO:16435 RGO:16440 Trueta phenomenon RGO:16440 renal tubular obstruction RGO:16441 renal tubular blockage RGO:16441 RGO:16443 striated nephrogram RGO:16443 SNOMEDCT:4876008 RGO:16444 acute obstruction RGO:16444 HP:0001919 SNOMEDCT:129561000119108 SNOMEDCT:14669001 RGO:16445 acute renal failure RGO:16445 Cacchi-Richi disease DOID:12713 ORDO:1309 RADLEX:RID34675 SNOMEDCT:236443009 RGO:16446 medullary sponge kidney RGO:16446 RGO:16447 renal tubular ectasia RGO:16447 RGO:16448 arterial emboli RGO:16448 RGO:16451 unilateral renal nonfunction RGO:16451 SNOMEDCT:95474000 RGO:16460 arteriovenous malformation of kidney RGO:16460 RGO:16463 nonfunction of part of kidney RGO:16463 RGO:16470 unilaterally decreased renal contrast concentration RGO:16470 RGO:16475 recent passage of ureteral calculus RGO:16475 RGO:16477 trauma with spasm of pelvocaliceal system RGO:16477 RGO:16479 bilaterally decreased renal contrast concentration RGO:16479 RGO:16487 Tamm-Horsfall proteinuria RGO:16487 RGO:16489 intrarenal contrast collection RGO:16489 RGO:16491 dilated calyx RGO:16491 RGO:16493 communicating urinoma RGO:16493 RGO:16496 clubbing or destruction of renal calyces RGO:16496 RGO:16497 obstruction of infundibulum RGO:16497 RGO:16499 vesicopelvic reflux RGO:16499 papillary necrosis SNOMEDCT:90241004 RGO:16502 renal papillary necrosis RGO:16502 RGO:16503 analgesic abuse RGO:16503 RGO:16504 obstruction of urinary tract RGO:16504 abscess of kidney carbuncle renal carbuncle renal cortical abscess SNOMEDCT:3321001 RGO:16505 renal abscess RGO:16505 infundibular stenosis RGO:16510 infundibular narrowing RGO:16510 RGO:16516 extrarenal pelvis RGO:16516 RGO:16522 filling defect in renal collecting system RGO:16522 RGO:16528 normal renal artery or vein impression RGO:16528 ICD10CM:N28.84 RADLEX:RID3546 SNOMEDCT:37779008 RGO:16534 pyelitis cystica RGO:16534 RADLEX:RID3322 SNOMEDCT:54002007 RGO:16536 saccular aneurysm RGO:16536 focal renal calcifcation RGO:16537 focal calcification in kidney RGO:16537 renal artery aneursym ICD10CM:I72.2 SNOMEDCT:36184004 RGO:16538 aneurysm of renal artery RGO:16538 DOID:14092 ICD10CM:I70.1 SNOMEDCT:45281005 RGO:16539 atherosclerosis of renal artery RGO:16539 SNOMEDCT:13713005 RGO:16550 thromboembolus RGO:16550 urinary calculus RADLEX:RID4996 RGO:16552 urinary tract calculus RGO:16552 HP:0003149 RGO:16557 hyperuricosuria RGO:16557 ICD10CM:E72.53 RGO:16558 oxaluria RGO:16558 RGO:16560 schistosomiasis haematobium RGO:16560 HP:0003159 ICD10CM:E72.53 SNOMEDCT:367621000119107 RGO:16571 hyperoxaluria RGO:16571 DOID:2977 ORDO:416 SNOMEDCT:17901006 RGO:16572 primary hyperoxaluria RGO:16572 SNOMEDCT:63539008 RGO:16574 calcium oxalate calculus RGO:16574 RGO:16575 calcium phosphate calculus RGO:16575 SNOMEDCT:52990007 RGO:16576 cystine calculus RGO:16576 RGO:16577 calculus of struvite plus calcium phosphate RGO:16577 SNOMEDCT:88295005 RGO:16578 uric acid calculus RGO:16578 RGO:16579 indinavir crystal calculus RGO:16579 mucoproteinaceous calculus SNOMEDCT:699321009 RGO:16580 matrix calculus RGO:16580 magnesium ammonium phosphate calculus SNOMEDCT:42851001 RGO:16581 struvite calculus RGO:16581 SNOMEDCT:7828002 RGO:16582 xanthine calculus RGO:16582 SNOMEDCT:20917003 RGO:16584 chronic glomerulonephritis RGO:16584 DOID:2973 HP:0025418 ICD10CM:N17.1 SNOMEDCT:444691002 RGO:16585 renal cortical necrosis RGO:16585 RGO:16586 AIDS-related infection RGO:16586 RGO:16590 methoxyflurane anesthesia RGO:16590 ICD10CM:E72.53 SNOMEDCT:373607009 RGO:16591 oxalosis RGO:16591 SNOMEDCT:236570004 RGO:16593 renal transplant rejection RGO:16593 HP:0003355 SNOMEDCT:35912001 RGO:16598 aminoaciduria RGO:16598 ORDO:112 SNOMEDCT:707742001 RGO:16599 Bartter syndrome RGO:16599 ORDO:94086 SNOMEDCT:59531002 RGO:16600 blue diaper syndrome RGO:16600 RGO:16601 dialysis therapy RGO:16601 DOID:13810 ICD10CM:E78.01 SNOMEDCT:398036000 RGO:16603 familial hypercholesterolemia RGO:16603 RGO:16605 hypochloremic acidosis RGO:16605 RGO:16606 idiopathic renal hypercalciuria RGO:16606 SNOMEDCT:90241004 RGO:16610 renal medullary necrosis RGO:16610 DOID:9620 HP:0000076 RADLEX:RID5261 SNOMEDCT:197811007 RGO:16612 vesicoureteral reflux RGO:16612 SNOMEDCT:84114007 RGO:16615 myocardial failure RGO:16615 RGO:16618 snakebite RGO:16618 SNOMEDCT:82545002 RGO:16619 transfusion reaction RGO:16619 simple renal cortical cyst SNOMEDCT:77945009 RGO:16621 simple renal cyst RGO:16621 RGO:16625 hydronephrotic multicystic kidney RGO:16625 RGO:16626 pyeloinfundibular atresia RGO:16626 HP:0100611 RGO:16631 glomerulocystic kidney disease RGO:16631 microcystic kidney disease RGO:16632 microcystic disease RGO:16632 cystic disease of kidney cystic kidneys RGO:16635 renal cystic disease RGO:16635 pyelogenic cyst SNOMEDCT:433036004 RGO:16636 calyceal diverticulum RGO:16636 RGO:16638 focal hydronephrosis RGO:16638 RGO:16643 cystic dysplasia of renal cortex RGO:16643 RGO:16644 endometrial cyst RGO:16644 SNOMEDCT:86463003 RGO:16647 multilocular renal cyst RGO:16647 RGO:16648 pericaliceal lymphangiectasis RGO:16648 AR-PKD ARPKD autosomal recessive polycystic renal disease infantile polycystic kidney disease DOID:0110861 DOID:5928 ORDO:731 SNOMEDCT:28770003 RGO:16649 autosomal recessive polycystic kidney disease RGO:16649 RGO:16650 congenital renal cystic disease RGO:16650 AD-PKD ADPKD adult-type polycystic renal disease autosomal dominant polycystic renal disease DOID:898 SNOMEDCT:28728008 RGO:16651 autosomal dominant polycystic kidney disease RGO:16651 RGO:16653 brachymesomelia-renal syndrome RGO:16653 ORDO:218 SNOMEDCT:48611009 RGO:16654 Darier disease RGO:16654 RGO:16656 Goldston syndrome RGO:16656 DOID:0050777 ORDO:475 RADLEX:RID34838 SNOMEDCT:716997004 RGO:16657 Joubert syndrome RGO:16657 ORDO:97366 RGO:16660 multiloculated cystic renal lesion RGO:16660 RGO:16664 localized renal cystic disease RGO:16664 RGO:16666 septated cyst RGO:16666 RGO:16668 bilateral or multiple cystic renal masses RGO:16668 RGO:16671 glomerulocystic disease RGO:16671 SNOMEDCT:427917002 RGO:16673 multiple abscesses RGO:16673 hyperdense renal cyst RGO:16674 high-density renal cyst RGO:16674 SNOMEDCT:248784000 SNOMEDCT:52321009 RGO:16676 hemorrhagic cyst RGO:16676 RGO:16677 focal renal parenchymal scar RGO:16677 RGO:16678 calyceal calculi RGO:16678 RGO:16682 depression in renal margin RGO:16682 RGO:16683 arterionephrosclerosis RGO:16683 fetal lobation RGO:16685 fetal lobulation RGO:16685 SNOMEDCT:60926001 RGO:16688 chronic interstitial nephritis RGO:16688 RGO:16689 localized bulge of renal outline RGO:16689 RGO:16691 localized hypertrophy with atrophy of remaining portion of kidney RGO:16691 RGO:16695 acute lobar pyelonephritis RGO:16695 RGO:16697 localized hydronephrosis RGO:16697 RGO:16698 renal pseudotumor RGO:16698 RADLEX:RID35177 RGO:16699 dromedary hump RGO:16699 HP:0000081 RGO:16700 duplicated collecting system RGO:16700 RGO:16701 lipomatosis of renal pelvis RGO:16701 RGO:16705 splenic imprint RGO:16705 RGO:16707 aberrant papilla RGO:16707 RGO:16708 renunculus RGO:16708 tumor of renal collecting system, pelvis, and ureter tumor of urothelium RGO:16709 urothelial tumor RGO:16709 DOID:0050685 RADLEX:RID4256 SNOMEDCT:74364000 RGO:16715 small cell carcinoma RGO:16715 RGO:16727 lymphohematogenous spread RGO:16727 tumor of renal parenchyma RGO:16728 renal parenchymal tumor RGO:16728 RCC hypernephroma DOID:4450 HP:0005584 RADLEX:RID4230 SNOMEDCT:41607009 SNOMEDCT:702391001 RGO:16734 renal cell carcinoma RGO:16734 RGO:16741 renal mass in a child RGO:16741 RGO:16745 fibroepithelial polyp of renal pelvis or ureter RGO:16745 RADLEX:RID4538 RGO:16747 multilocular cystic renal tumor RGO:16747 RGO:16748 ossifying renal tumor of infancy RGO:16748 SNOMEDCT:4135001 RGO:16752 aniridia-Wilms tumor association RGO:16752 RGO:16754 neonatal renal mass RGO:16754 RGO:16758 solid renal mass RGO:16758 TCC DOID:2671 RADLEX:RID4279 SNOMEDCT:27090000 RGO:16771 transitional cell carcinoma RGO:16771 RGO:16773 cystic renal mass RGO:16773 RGO:16780 cystic hematoma RGO:16780 RGO:16784 cystic renal mass with internal debris RGO:16784 RGO:16787 infected cyst RGO:16787 RGO:16789 cystic renal mass with wall calcification RGO:16789 RGO:16793 renal mass with calcification RGO:16793 RGO:16794 calcified stone with hydronephrosis RGO:16794 renal mass with fat RGO:16800 fat-containing renal mass RGO:16800 DOID:12143 HP:0000011 RADLEX:RID5298 SNOMEDCT:398064005 RGO:16802 neurogenic bladder RGO:16802 SNOMEDCT:54768000 RGO:16808 bladder distention RGO:16808 RGO:16810 diuretic medication RGO:16810 SNOMEDCT:95571006 RGO:16815 renal hemorrhage RGO:16815 RGO:16821 renal parenchymal gas RGO:16821 RGO:16822 emphysematous pylenonephritis RGO:16822 RGO:16824 nephrointestinal fistula RGO:16824 RGO:16826 chronic renal infection RGO:16826 RGO:16830 dark kidney on T2 MRI RGO:16830 RGO:16831 multiple blood transfusions RGO:16831 lesion involving perirenal space RGO:16832 lesion of perinephric space RGO:16832 RGO:16833 invasive colon cancer RGO:16833 RGO:16841 perirenal fluid collection RGO:16841 RGO:16842 loculated ascites RGO:16842 RGO:16847 gas abscess RGO:16847 DOID:5200 RADLEX:RID34394 SNOMEDCT:7163005 RGO:16849 obstructive uropathy RGO:16849 perinephric hemorrhage SNOMEDCT:197824007 RGO:16854 perinephric hematoma RGO:16854 SNOMEDCT:45456005 RGO:16864 infarction of kidney RGO:16864 renal sinus leakage RGO:16868 peripelvic extravasation RGO:16868 RGO:16874 peripheral rim enhancement of kidney RGO:16874 RGO:16876 severe hydronephrosis RGO:16876 RGO:16877 acute renal artery occlusion RGO:16877 RGO:16878 acute renal vein thrombosis RGO:16878 RGO:16879 renal ischemia RGO:16879 SNOMEDCT:90493000 RGO:16880 arteriolar nephrosclerosis RGO:16880 DOID:1076 SNOMEDCT:63302006 RGO:16881 chronic pyelonephritis RGO:16881 RGO:16887 renal artery aneurysm RGO:16887 RGO:16895 extrinsic pressure from adjacent mass RGO:16895 SNOMEDCT:213148006 RGO:16898 transplant rejection RGO:16898 RGO:16908 renal artery aneurysm or microaneurysm RGO:16908 RGO:16915 drug abuse angiitis RGO:16915 RGO:16917 rheumatic or rheumatoid arteritis RGO:16917 SNOMEDCT:110421000 RGO:16918 traumatic aneurysm RGO:16918 RGO:16920 avascular renal mass RGO:16920 RGO:16925 early renal vein opacification RGO:16925 thromboembolism of renal vein thrombosis of renal vein SNOMEDCT:15842009 RGO:16931 renal vein thrombosis RGO:16931 RGO:16937 ascending phlebitis RGO:16937 SNOMEDCT:707221002 RGO:16939 diabetic glomerulosclerosis RGO:16939 DOID:1073 RADLEX:RID3313 SNOMEDCT:28119000 RGO:16941 renal hypertension RGO:16941 echo-free renal mass RGO:16942 anechoic renal mass RGO:16942 ICD10CM:N13.6 RADLEX:RID3548 SNOMEDCT:48631008 RGO:16951 pyonephrosis RGO:16951 RGO:16952 tuberculous cavity RGO:16952 RGO:16953 hypoechoic renal mass RGO:16953 RGO:16954 abscess with debris RGO:16954 RGO:16955 renal cyst with debris RGO:16955 RGO:16956 calyceal diverticulum with debris RGO:16956 RGO:16959 localized hydronephrosis with debris RGO:16959 RGO:16960 isoechoic renal mass RGO:16960 RGO:16961 hypertrophied column of Bertin RGO:16961 RGO:16964 hyperechoic renal mass RGO:16964 RGO:16968 abscess with microbubble gas formation RGO:16968 RGO:16972 focal renal dysplasia RGO:16972 RGO:16974 hypertrophied column of Bertin viewed en face RGO:16974 RGO:16975 infarct with focal scar RGO:16975 RGO:16978 multilocular or complex renal mass RGO:16978 RGO:16979 cystic Wilms tumor RGO:16979 RGO:16980 necrotic tumor with debris RGO:16980 RGO:16984 segmental cystic disease RGO:16984 RGO:16989 malacoplakia of renal parenchyma RGO:16989 RGO:16993 sonographically ill-defined renal parenchymal mass RGO:16993 RGO:16996 shadowing mass in renal collecting system RGO:16996 RGO:17001 transitional cell carcinoma with calcification RGO:17001 hypoechoic renal cortex RGO:17002 decreased renal cortical echogenicity RGO:17002 RGO:17003 multicentric renal cell carcinoma RGO:17003 DOID:0080162 SNOMEDCT:68815009 RGO:17004 lupus nephritis RGO:17004 hyperechoic renal cortex with normal medulla RGO:17005 hyperechoic renal cortex RGO:17005 SNOMEDCT:28637003 RGO:17006 acute interstitial nephritis RGO:17006 DOID:2370 SNOMEDCT:127013003 RGO:17008 diabetic nephropathy RGO:17008 DOID:11664 HP:0009741 SNOMEDCT:32916005 RGO:17010 nephrosclerosis RGO:17010 DOID:0080108 HP:0002913 ICD10CM:R82.1 SNOMEDCT:48165008 RGO:17012 myoglobinuria RGO:17012 DOID:10591 HP:0100602 ICD10CM:O14 ORDO:275555 SNOMEDCT:398254007 RGO:17015 pre-eclampsia RGO:17015 RGO:17016 hyperechoic renal medulla RGO:17016 RGO:17018 renal pyramidal fibrosis RGO:17018 RGO:17020 pseudo-Bartter syndrome RGO:17020 HP:0008682 ICD10CM:N17.0 RGO:17022 renal tubular necrosis RGO:17022 echogenic kidney hyperechoic kidney hyperechoic renal cortex and medulla RGO:17023 hyperechoic renal parenchyma RGO:17023 RGO:17027 renal collecting system echoes RGO:17027 SNOMEDCT:236373001 RGO:17028 emphysematous pyelonephritis RGO:17028 RGO:17031 increased renal artery diastolic flow RGO:17031 RGO:17034 decreased renal artery diastolic flow RGO:17034 DOID:11823 ICD10CM:K76.7 SNOMEDCT:51292008 RGO:17037 hepatorenal syndrome RGO:17037 RGO:17041 increased resistance index of renal transplant RGO:17041 RGO:17043 acute cyclosporine nephrotoxicity RGO:17043 kidney compressed by perirenal collection kidney compressed by subcapsular collection ICD10CM:N26.2 RADLEX:RID35413 SNOMEDCT:367821000119106 RGO:17047 Page kidney RGO:17047 enlarged renal transplant enlarged transplant kidney RGO:17049 enlargement of renal transplant RGO:17049 small renal transplant RGO:17053 diminished size of renal transplant RGO:17053 RGO:17054 chronic transplant rejection RGO:17054 diminished function of transplanted kidney RGO:17056 decreased renal transplant function RGO:17056 RGO:17057 cyclosporine toxicity RGO:17057 RGO:17059 renal arterial insufficiency RGO:17059 RGO:17083 medial deviation of upper ureter RGO:17083 RGO:17092 tortuous aorta RGO:17092 RGO:17094 lateral deviation of upper ureter RGO:17094 RGO:17106 displacement of pelvic ureter RGO:17106 SNOMEDCT:111367007 RGO:17107 pelvic abscess RGO:17107 DOID:13254 SNOMEDCT:111359004 RGO:17109 diverticulitis of colon RGO:17109 RGO:17114 pelvic hernia RGO:17114 RGO:17115 ureteral and renal pelvic calcification RGO:17115 RGO:17123 intraluminal ureteral filling defect RGO:17123 RADLEX:RID3677 SNOMEDCT:472816004 RGO:17128 eosinophilic ureteritis RGO:17128 RGO:17131 sloughed papilla from papillary necrosis RGO:17131 ICD10CM:N28.86 RADLEX:RID3676 SNOMEDCT:37779008 RGO:17132 ureteritis cystica RGO:17132 RGO:17133 mural ureteral filling defect RGO:17133 DOID:11885 RGO:17142 ureteral tumor RGO:17142 DOID:6873 RADLEX:RID3883 SNOMEDCT:31069005 RGO:17145 fibroepithelial polyp RGO:17145 RGO:17148 multiple ureteral filling defects RGO:17148 SNOMEDCT:125244003 RGO:17150 multiple calculi RGO:17150 RGO:17156 vascular indentation on ureter or renal pelvis RGO:17156 RGO:17159 normal accessory renal artery RGO:17159 RGO:17160 normal iliac artery RGO:17160 RGO:17162 arteriovenous communication of renal or juxtarenal vessels RGO:17162 RGO:17163 cirsoid aneurysm of renal artery RGO:17163 RGO:17165 normal gonadal vein RGO:17165 RGO:17169 mid-ureteral spindle proximal to iliac artery crossing RGO:17169 RGO:17172 ureteral duplication with obstruction RGO:17172 DOID:4022 HP:0000070 RADLEX:RID34640 SNOMEDCT:12818004 RGO:17173 ureterocele RGO:17173 RGO:17177 ureterovesical surgery RGO:17177 RGO:17178 anomaly of ureterovesical junction RGO:17178 RGO:17180 duplication of ureters RGO:17180 RGO:17181 ectopic ureter emptying into bladder neck or urethra RGO:17181 RGO:17183 megaureter-megacystis syndrome RGO:17183 obstructed ureter ureteral obstruction SNOMEDCT:20018005 RGO:17187 obstruction of ureter RGO:17187 RGO:17195 vascular compression of ureter RGO:17195 RGO:17196 Hutch diverticulum RGO:17196 RGO:17199 papillary necrosis with sloughed papilla RGO:17199 SNOMEDCT:25341005 RGO:17201 ureteral stricture RGO:17201 RGO:17205 xanthogranulomatous stricture RGO:17205 RGO:17206 ureteral extravasation or fistula RGO:17206 RGO:17212 calculus in bladder neck RGO:17212 RGO:17214 infrequent voiding RGO:17214 DOID:11132 SNOMEDCT:266569009 RGO:17217 prostatic hypertrophy RGO:17217 RGO:17220 foreign body obstruction RGO:17220 ICD10CM:Q62.32 SNOMEDCT:253894005 RGO:17223 ectopic ureterocele RGO:17223 RGO:17230 pelvic hematoma or hemorrhage RGO:17230 RGO:17232 recent voiding RGO:17232 RADLEX:RID5302 SNOMEDCT:236635009 RGO:17237 detrusor areflexia RGO:17237 RGO:17238 detrusor hyperreflexia/detrusor-external sphincter dyssynergia RGO:17238 RGO:17239 idiopathic uninhibited bladder RGO:17239 RGO:17240 neoplasm of spine, spinal cord, or brain RGO:17240 RGO:17241 paralyic disorder RGO:17241 RGO:17242 spina bifida vera with meningomyelocele RGO:17242 RADLEX:RID5161 SNOMEDCT:26039008 RGO:17244 neurosyphilis RGO:17244 DOID:1572 HP:0002343 ORDO:314928 RADLEX:RID4889 SNOMEDCT:30753002 RGO:17245 normal pressure hydrocephalus RGO:17245 RADLEX:RID3502 SNOMEDCT:16631009 RGO:17246 transverse myelitis RGO:17246 extrinsic bladder deformity extrinsic deformity of bladder RGO:17248 extrinsic pressure deformity of bladder RGO:17248 ICD10CM:I72.3 SNOMEDCT:13290008 RGO:17257 aneurysm of iliac artery RGO:17257 RGO:17258 anterior myelomeningocele RGO:17258 RGO:17265 rheumatoid synovial cyst of hip joint RGO:17265 RGO:17266 urachal remnant RGO:17266 RGO:17267 urethral neoplasm RGO:17267 HP:0100650 RGO:17268 vaginal neoplasm RGO:17268 RGO:17269 focal bladder wall thickening RGO:17269 RGO:17271 invasion by adjacent tumor RGO:17271 RGO:17273 adjacent abscess RGO:17273 RGO:17277 generalized bladder wall thickening RGO:17277 DOID:1679 ICD10CM:N30 RADLEX:RID3405 SNOMEDCT:38822007 RGO:17282 cystitis RGO:17282 Cytoxan cystitis RGO:17285 cyclophosphamide cystitis RGO:17285 cystitis glandularis DOID:7138 RADLEX:RID3704 SNOMEDCT:13285005 RGO:17286 cystitis cystica RGO:17286 RADLEX:RID3703 SNOMEDCT:445918001 RGO:17287 eosinophilic cystitis RGO:17287 DOID:13949 ORDO:37202 SNOMEDCT:197834003 RGO:17288 interstitial cystitis RGO:17288 HP:0009725 RGO:17289 bladder tumor RGO:17289 RGO:17293 mesenchymal neoplasm RGO:17293 SNOMEDCT:274730004 RGO:17295 bladder filling defect RGO:17295 RGO:17301 Brunn nest RGO:17301 RGO:17302 condyloma acuminata RGO:17302 DOID:7334 RADLEX:RID4219 SNOMEDCT:78236000 RGO:17308 nephrogenic adenoma RGO:17308 RGO:17311 prolapsing urethral polyp RGO:17311 RADLEX:RID3810 SNOMEDCT:83577005 RGO:17313 squamous metaplasia RGO:17313 RGO:17314 calcification in bladder wall or lumen RGO:17314 DOID:9266 HP:0003131 ICD10CM:E72.01 ORDO:214 SNOMEDCT:85020001 RGO:17319 cystinuria RGO:17319 RGO:17327 radiation reaction RGO:17327 bladder stone cystolith urinary bladder calculus DOID:11355 RADLEX:RID5008 SNOMEDCT:70650003 RGO:17328 bladder calculus RGO:17328 BOO obstruction of bladder SNOMEDCT:416991005 RGO:17329 bladder outlet obstruction RGO:17329 RGO:17330 chronic catheterization RGO:17330 RGO:17331 urea-splitting microorganisms RGO:17331 RGO:17332 bladder wall sutures RGO:17332 RGO:17333 gas in bladder wall or lumen RGO:17333 HP:0004321 SNOMEDCT:68666001 RGO:17334 bladder fistula RGO:17334 RGO:17339 fungus ball in bladder RGO:17339 RGO:17340 congenital anal atresia RGO:17340 RGO:17344 calculus eroding through bladder wall RGO:17344 RGO:17345 tuberculous enterocolitis RGO:17345 diverticulum of bladder urinary bladder diverticulum DOID:11353 HP:0000015 SNOMEDCT:197866008 RGO:17346 bladder diverticulum RGO:17346 RGO:17350 bladder sphincter dyssynergia RGO:17350 RGO:17359 urinary tract obstruction below the bladder in a child RGO:17359 SNOMEDCT:197919005 RGO:17360 meatal stenosis RGO:17360 stricture of urethra DOID:1829 HP:0012227 ICD10CM:N35 SNOMEDCT:76618002 RGO:17361 urethral stricture RGO:17361 RGO:17364 normal folds RGO:17364 DOID:9341 HP:0008722 ICD10CM:N36.1 SNOMEDCT:90531003 RGO:17366 urethral diverticulum RGO:17366 RGO:17367 urethral polyp RGO:17367 DOID:1343 HP:0500006 SNOMEDCT:31822004 RGO:17368 urethritis RGO:17368 RGO:17369 verumontanum hypertrophy RGO:17369 stricture of anterior urethra RGO:17370 anterior urethral stricture RGO:17370 DOID:13477 ICD10CM:N48.0 SNOMEDCT:198033005 RGO:17374 balanitis xerotica obliterans RGO:17374 RGO:17376 dilated posterior urethra RGO:17376 HP:0010957 ORDO:93110 RADLEX:RID34697 SNOMEDCT:253900005 RGO:17378 posterior urethral valve RGO:17378 RGO:17379 previous prostatectomy RGO:17379 SNOMEDCT:126883004 RGO:17380 urethral tumor RGO:17380 DOID:3172 SNOMEDCT:86143001 RGO:17382 papillary adenoma RGO:17382 DOID:2670 SNOMEDCT:45083001 RGO:17383 transitional cell papilloma RGO:17383 RGO:17386 urethral filling defect RGO:17386 RGO:17400 urethral outpouching RGO:17400 RADLEX:RID257 RGO:17405 Cowper glands RGO:17405 HP:0010481 RGO:17408 urethral valve RGO:17408 HP:0010480 ICD10CM:N36.0 SNOMEDCT:14981000 RGO:17409 urethral fistula RGO:17409 DOID:7551 SNOMEDCT:15628003 RGO:17411 gonorrhea RGO:17411 RGO:17412 unilateral adrenal enlargement RGO:17412 DOID:4817 HP:0003005 ORDO:251992 RADLEX:RID4458 SNOMEDCT:116371000119107 SNOMEDCT:53801007 RGO:17414 ganglioneuroma RGO:17414 RADLEX:RID3777 SNOMEDCT:76197007 RGO:17415 hyperplasia RGO:17415 RGO:17418 carcinoma of adrenal cortex RGO:17418 RGO:17424 bilateral adrenal enlargement RGO:17424 RGO:17427 neuroblastomas RGO:17427 RGO:17431 cystic adrenal lesion RGO:17431 RGO:17433 endothelial cyst RGO:17433 RGO:17434 lymphatic cyst RGO:17434 RADLEX:RID3954 SNOMEDCT:13467000 RGO:17435 pseudocyst RGO:17435 SNOMEDCT:127021009 RGO:17436 adrenal tumor RGO:17436 adrenal carcinoma DOID:3948 HP:0006744 ORDO:1501 RGO:17439 adrenocortical carcinoma RGO:17439 RGO:17441 adrenal pseudotumor RGO:17441 RADLEX:RID175 RGO:17442 pancreatic tail RGO:17442 RGO:17443 pseudomyelolipoma RGO:17443 RGO:17445 stomach fundus RGO:17445 RGO:17446 upper pole renal neoplasms RGO:17446 SNOMEDCT:75198005 RGO:17447 diverticulum of stomach RGO:17447 SNOMEDCT:13568007 RGO:17448 duplication of stomach RGO:17448 RGO:17449 hepatic mass RGO:17449 DOID:9931 ICD10CM:A39.1 ORDO:100067 SNOMEDCT:36102002 RGO:17453 Waterhouse-Friderichsen syndrome RGO:17453 SNOMEDCT:239892009 RGO:17456 primary antiphospholipid syndrome RGO:17456 hypoadrenalism HP:0000846 SNOMEDCT:386584007 RGO:17458 adrenal insufficiency RGO:17458 RGO:17460 withdrawal of exogenous steroids RGO:17460 RGO:17463 exogenous steroids RGO:17463 RGO:17464 hyperplasia from pituitary or ectopic ACTH RGO:17464 DOID:656 SNOMEDCT:255036008 RGO:17465 adrenal adenoma RGO:17465 HP:0002666 RADLEX:RID4516 SNOMEDCT:302835009 SNOMEDCT:85583005 RGO:17466 pheochromocytoma RGO:17466 ORDO:139411 RGO:17467 Carney triad RGO:17467 RGO:17469 aneurysm of abdominal aorta or its branches RGO:17469 RGO:17480 hemorrhage, traumatic or bleeding disorder RGO:17480 RGO:17484 retroperitoneal extension of scirrhous or desmoplastic carcinoma of stomach, colon, or prostate RGO:17484 RGO:17486 sclerosing agent for hemorrhoids RGO:17486 RGO:17492 enlarged iliopsoas muscle RGO:17492 DOID:3627 SNOMEDCT:73067008 RGO:17498 ruptured aortic aneurysm RGO:17498 RGO:17501 metastatic lymphadenopathy RGO:17501 atrophy of contralateral psoas muscle RGO:17505 pseudoenlargement of psoas muscle RGO:17505 RGO:17507 cystic retroperitoneal mass RGO:17507 RADLEX:RID4163 RGO:17511 pancreatic cystic neoplasm RGO:17511 RGO:17512 cystic retroperitoneal lymphadenopathy RGO:17512 RGO:17518 pneumatosis intestinalis with leakage RGO:17518 large soft-tissue mass in pelvis RGO:17520 large pelvic soft-tissue mass RGO:17520 RGO:17521 feces in colon RGO:17521 HP:0000125 RADLEX:RID3747 SNOMEDCT:56108007 RGO:17531 pelvic kidney RGO:17531 RGO:17534 solid pelvic mass RGO:17534 HP:0010784 RGO:17539 uterine neoplasm RGO:17539 RGO:17546 cystic pelvic mass RGO:17546 SNOMEDCT:703077007 RGO:17550 paraovarian cyst RGO:17550 DOID:11612 HP:0000147 RGO:17555 polycystic ovary RGO:17555 RGO:17556 complex pelvic mass RGO:17556 ICD10CM:N83.1 RGO:17558 hemorrhagic corpus luteum cyst RGO:17558 SNOMEDCT:88981003 RGO:17564 pyometrium RGO:17564 RGO:17566 pelvic mass in an infant or child RGO:17566 dilatation of ureter dilated ureter ureterectasis HP:0000072 ICD10CM:N13.4 SNOMEDCT:69758005 RGO:17573 hydroureter RGO:17573 RGO:17580 lower abdominal calcification RGO:17580 HP:0009725 RGO:17591 bladder neoplasm RGO:17591 RGO:17605 abnormal gas collection in pelvis RGO:17605 vaginitis emphysematosa SNOMEDCT:8628002 RGO:17612 emphysematous vaginitis RGO:17612 RGO:17617 intestinal necrosis RGO:17617 prostatic enlargement prostatomegaly SNOMEDCT:249607009 RGO:17620 enlarged prostate RGO:17620 BPH HP:0008711 ICD10CM:N40 RADLEX:RID3784 SNOMEDCT:266569009 RGO:17621 benign prostatic hyperplasia RGO:17621 DOID:14654 HP:0000024 RADLEX:RID3544 SNOMEDCT:9713002 RGO:17622 prostatitis RGO:17622 RGO:17623 anechoic prostate lesion RGO:17623 RGO:17625 ejaculatory duct cyst RGO:17625 RGO:17626 seminal vesicle cyst RGO:17626 RGO:17629 cystic carcinoma of prostate RGO:17629 HP:0100645 ICD10CM:N81.1 RADLEX:RID4788 SNOMEDCT:252005008 RGO:17630 cystocele RGO:17630 utricular cyst RGO:17631 utricle cyst RGO:17631 RGO:17632 hypoechoic prostate lesion RGO:17632 RGO:17634 atypical prostatic hyperplasia RGO:17634 RGO:17637 complex cyst RGO:17637 RADLEX:RID3820 SNOMEDCT:112674009 SNOMEDCT:263756000 RGO:17638 fibrosis RGO:17638 RGO:17640 isoechoic prostate lesion RGO:17640 RGO:17641 atypical hyperplasia of prostate RGO:17641 ICD10CM:N41.4 SNOMEDCT:61500009 RGO:17642 granulomatous prostatitis RGO:17642 RGO:17643 hyperechoic prostate lesion RGO:17643 ICD10CM:N41.1 SNOMEDCT:19905009 RGO:17644 chronic prostatitis RGO:17644 RGO:17645 comedocarcinoma of prostate RGO:17645 RGO:17646 hypervascular prostate lesion RGO:17646 RGO:17649 T2-hypointense peripheral zone of prostate RGO:17649 RGO:17652 intraepithelial neoplasia of prostate RGO:17652 RGO:17653 post-hormonal therapy RGO:17653 low-intensity seminal vesicle on T2 image RGO:17654 T2-dark seminal vesicle RGO:17654 DOID:9365 SNOMEDCT:27001009 RGO:17657 seminal vesiculitis RGO:17657 RGO:17658 cystic structure near seminal vesicle RGO:17658 RGO:17659 müllerian remnant cyst RGO:17659 RGO:17663 chronic nonspecific infection RGO:17663 RGO:17665 abnormality of entire testis RGO:17665 DOID:2518 HP:0100796 ICD10CM:N45.2 SNOMEDCT:274718005 RGO:17666 orchitis RGO:17666 DOID:11383 HP:0000028 SNOMEDCT:127907005 SNOMEDCT:204878001 RGO:17668 undescended testis RGO:17668 RGO:17671 solid testicular mass RGO:17671 HP:0010788 RGO:17673 testicular neoplasm RGO:17673 RGO:17674 cystic testicular mass RGO:17674 RGO:17675 cystic dysplasia RGO:17675 RGO:17679 tunica albuginea cyst RGO:17679 RGO:17680 unilateral testicular tumor RGO:17680 RADLEX:RID4250 RGO:17681 embryonal cell carcinoma RGO:17681 yolk sac tumor DOID:1911 RADLEX:RID4326 SNOMEDCT:74409009 RGO:17682 endodermal sinus tumor RGO:17682 DOID:4440 RADLEX:RID4316 SNOMEDCT:36741007 SNOMEDCT:443675005 RGO:17683 seminoma RGO:17683 DOID:2696 SNOMEDCT:5014008 RGO:17685 Leydig cell tumor RGO:17685 DOID:3577 SNOMEDCT:128857001 RGO:17686 Sertoli cell tumor RGO:17686 RGO:17687 bilateral testicular masses RGO:17687 RGO:17690 adrenal rest hyperplasia RGO:17690 testicular germ cell tumor RGO:17691 germ cell testicular tumor RGO:17691 MGCT ORDO:180234 RADLEX:RID4328 SNOMEDCT:32844007 RGO:17692 mixed germ cell tumor RGO:17692 ORDO:180229 SNOMEDCT:28325008 RGO:17693 polyembryoma RGO:17693 DOID:5834 ORDO:99865 RADLEX:RID4317 SNOMEDCT:9294008 RGO:17694 spermatocytic seminoma RGO:17694 RGO:17695 non-germ cell testicular tumor RGO:17695 DOID:1786 SNOMEDCT:54292009 RGO:17696 adrenal rest tumor RGO:17696 DOID:14544 RGO:17697 adenocarcinoma of rete testis RGO:17697 DOID:3301 HP:0000150 SNOMEDCT:74751003 RGO:17698 gonadoblastoma RGO:17698 DOID:2999 SNOMEDCT:46585005 RGO:17699 granulosa cell tumor RGO:17699 RGO:17700 papillary adenocarcinoma of rete testis RGO:17700 RGO:17701 testicular tumor in a child RGO:17701 RGO:17703 testicular calcification RGO:17703 RGO:17706 spermatic granuloma RGO:17706 lesion of epididymis RGO:17711 epididymal lesion RGO:17711 DOID:746 SNOMEDCT:2348006 RGO:17712 adenomatoid tumor RGO:17712 DOID:9402 HP:0000031 ICD10CM:N45.1 SNOMEDCT:31070006 RGO:17713 epididymitis RGO:17713 DOID:11997 RADLEX:RID3939 SNOMEDCT:49263001 RGO:17714 spermatocele RGO:17714 scrotal mass RGO:17716 mass in scrotum RGO:17716 DOID:9912 HP:0000034 RADLEX:RID3912 SNOMEDCT:386152007 SNOMEDCT:55434001 RGO:17718 hydrocele RGO:17718 benign testicular hypertrophy RGO:17722 benign hypertrophy of testis RGO:17722 RGO:17728 extratesticular tumor in scrotum RGO:17728 RGO:17730 rhabdomyosarcoma of spermatic cord RGO:17730 RGO:17733 myxochondrosarcoma RGO:17733 RGO:17734 solid extratesticular mass in scrotum RGO:17734 RGO:17737 cystic extratesticular mass in scrotum RGO:17737 HP:0030424 SNOMEDCT:43077002 RGO:17738 epididymal cyst RGO:17738 RGO:17739 post vasectomy RGO:17739 RGO:17740 calcifications in scrotum RGO:17740 SNOMEDCT:403571009 RGO:17745 idiopathic scrotal calcinosis RGO:17745 DOID:5104 SNOMEDCT:33793000 RGO:17746 infarction of testis RGO:17746 RGO:17750 postinflammatory scrotal pearl RGO:17750 HP:0000029 SNOMEDCT:17585008 RGO:17751 testicular atrophy RGO:17751 calcification in vas deferens RGO:17752 vas deferens calcification RGO:17752 RGO:17753 fluid collection in scrotum RGO:17753 RGO:17756 hypospadias or ambiguous external genitalia RGO:17756 DOID:10892 ORDO:440 RGO:17758 familial hypospadias RGO:17758 Denys-Drash syndrome Drash syndrome HP:0000037 SNOMEDCT:111332007 RGO:17760 male pseudohermaphroditism RGO:17760 RGO:17762 calcifications in female genital tract RGO:17762 RGO:17766 arcuate arteries RGO:17766 RADLEX:RID34557 SNOMEDCT:181455002 SNOMEDCT:78067005 RGO:17768 placenta RGO:17768 DOID:0050166 SNOMEDCT:49558004 RGO:17770 tuberculous salpingitis RGO:17770 HP:0004320 RGO:17771 vaginal fistula RGO:17771 RGO:17779 osteomyelitis of pelvic bones RGO:17779 DOID:2170 HP:0030683 SNOMEDCT:30800001 RGO:17780 vaginitis RGO:17780 RGO:17787 hyperechoic focal uterine lesion RGO:17787 RGO:17788 calcified arcuate artery RGO:17788 RPOC SNOMEDCT:371374003 RGO:17793 retained products of conception RGO:17793 diffuse uterine enlargement RGO:17794 diffusely enlarged uterus RGO:17794 RGO:17795 carcinoma of endometrium RGO:17795 RGO:17797 multiparity RGO:17797 RGO:17798 normal parous uterus RGO:17798 RGO:17799 postpartum uterus RGO:17799 RGO:17800 recent abortion RGO:17800 RGO:17802 arteriovenous malformation involving uterus RGO:17802 SNOMEDCT:254877001 RGO:17807 sarcoma of uterus RGO:17807 RGO:17809 endometrial thickening RGO:17809 RGO:17810 early pregnancy RGO:17810 GTD gestational trophoblastic tumor trophoblastic tumor ORDO:59305 SNOMEDCT:416402001 SNOMEDCT:609518007 RGO:17811 gestational trophoblastic disease RGO:17811 DOID:9958 ICD10CM:N85.7 SNOMEDCT:38280009 RGO:17812 hematometra RGO:17812 SNOMEDCT:169413002 RGO:17813 hormone therapy RGO:17813 missed Ab ICD10CM:O02.1 SNOMEDCT:16607004 RGO:17815 missed abortion RGO:17815 RGO:17816 normal secretory phase RGO:17816 RGO:17818 pyometria RGO:17818 RGO:17819 tamoxifen therapy RGO:17819 RGO:17820 endometrial fluid RGO:17820 RGO:17821 cervical stenosis RGO:17821 RGO:17824 hematometrocolpos RGO:17824 HP:0030011 ICD10CM:Q52.3 SNOMEDCT:65937002 RGO:17825 imperforate hymen RGO:17825 RGO:17828 polyps of endometrium RGO:17828 SNOMEDCT:88981003 RGO:17830 pyometra RGO:17830 RGO:17831 duplication anomaly with obstruction RGO:17831 silhouette sign uterine silhouette sign RADLEX:RID35303 RGO:17833 indefinite uterus sign RGO:17833 SNOMEDCT:17433009 RGO:17836 ruptured ectopic pregnancy RGO:17836 prominent central uterine echo RGO:17837 prominence of central uterine echo RGO:17837 hyperplasia of endometrium ICD10CM:N85.0 SNOMEDCT:237072009 RGO:17838 endometrial hyperplasia RGO:17838 IUD contraceptive IUD contraceptive intrauterine device intrauterine contraceptive device RADLEX:RID34575 RGO:17841 intrauterine device RGO:17841 RGO:17843 normal menstrual endometrium RGO:17843 endometrial atrophy SNOMEDCT:301455002 SNOMEDCT:56699007 RGO:17847 atrophic endometrium RGO:17847 RGO:17851 cervical mass RGO:17851 cervical fibroid cervical leiomyoma fibroid of cervix RGO:17852 leiomyoma of cervix RGO:17852 RADLEX:RID3921 SNOMEDCT:24565001 RGO:17853 nabothian cyst RGO:17853 RGO:17854 free fluid in cul-de-sac RGO:17854 ruptured follicle ruptured ovarian follicle RGO:17855 follicular rupture RGO:17855 SNOMEDCT:34008004 RGO:17857 ovulation RGO:17857 RGO:17859 fallopian tube mass RGO:17859 RGO:17860 paratubal cyst RGO:17860 RGO:17861 cystic adnexal mass RGO:17861 DOID:13050 ICD10CM:N83.1 SNOMEDCT:386762009 RGO:17864 corpus luteum cyst RGO:17864 ICD10CM:K09.0 SNOMEDCT:103614000 SNOMEDCT:9245008 RGO:17865 follicular cyst RGO:17865 RGO:17868 peritoneal inclusion cyst RGO:17868 RGO:17869 theca lutein cyst RGO:17869 RGO:17870 complex cystic adnexal mass RGO:17870 DOID:1963 HP:0030394 RGO:17874 fallopian tube carcinoma RGO:17874 DOID:11612 SNOMEDCT:69878008 RGO:17877 polycystic ovary syndrome RGO:17877 RGO:17879 adnexal lesion with high diastolic flow RGO:17879 DOID:2683 RADLEX:RID4284 SNOMEDCT:2962009 RGO:17880 adenofibroma RGO:17880 RGO:17882 luteal cyst RGO:17882 RGO:17883 luteal phase of functioning ovary RGO:17883 RGO:17886 solid ovarian tumor RGO:17886 RADLEX:RID4286 SNOMEDCT:74739000 RGO:17887 Brenner tumor RGO:17887 DOID:4441 HP:0100621 RADLEX:RID4318 SNOMEDCT:60718004 RGO:17888 dysgerminoma RGO:17888 SNOMEDCT:254865006 RGO:17889 fibroma of ovary RGO:17889 DOID:2146 SNOMEDCT:423627007 RGO:17891 sarcoma of ovary RGO:17891 DOID:2997 SNOMEDCT:128905000 RGO:17892 Sertoli-Leydig cell tumor RGO:17892 RADLEX:RID4562 SNOMEDCT:52490000 RGO:17893 thecoma RGO:17893 RGO:17894 ovarian neoplasm or cyst in a child RGO:17894 RGO:17900 granulosa-thecal cell tumor RGO:17900 SNOMEDCT:28307001 SNOMEDCT:402878003 RGO:17902 germ cell tumor RGO:17902 RGO:17906 teratoma with malignant elements RGO:17906 RGO:17931 parenchymal brain hemorrhage RGO:17931 A-V malformation AV malformation AVM DOID:11294 HP:0100026 RADLEX:RID3334 SNOMEDCT:234141001 SNOMEDCT:24551003 RGO:17935 arteriovenous malformation RGO:17935 dural venous sinus thrombosis RGO:17947 dural sinus thrombosis RGO:17947 DOID:3755 HP:0001976 ICD10CM:D68.59 SNOMEDCT:36351005 RGO:17948 antithrombin III deficiency RGO:17948 HP:0025343 ICD10CM:D68.62 SNOMEDCT:16923002 SNOMEDCT:19267009 RGO:17950 lupus anticoagulant RGO:17950 RGO:17951 malignant neoplasm invasion RGO:17951 HP:0005318 SNOMEDCT:427020007 RGO:17953 cerebral vasculitis RGO:17953 DOID:9809 SNOMEDCT:60555002 RGO:17957 hypersensitivity vasculitis RGO:17957 RGO:17958 hypocomplemenemic vasculitis RGO:17958 RGO:17959 malignancy with vasculitis RGO:17959 ICD10CM:D89.1 RGO:17960 mixed cryoglobulinemia RGO:17960 RGO:17963 systemic necrotizing vasculitis RGO:17963 DOID:2555 RGO:17965 granulomatous angiitis RGO:17965 RGO:17968 bowel bypass dermatitis RGO:17968 RGO:18003 subependymal tumor spread RGO:18003 HP:0012174 HP:0100843 ORDO:360 SNOMEDCT:63634009 RGO:18004 glioblastoma RGO:18004 globoid cell leukodystrophy DOID:10587 ICD10CM:E75.23 ORDO:487 SNOMEDCT:192782005 RGO:18031 Krabbe disease RGO:18031 DOID:3210 ORDO:702 SNOMEDCT:64855000 RGO:18033 Pelizaeus-Merzbacher disease RGO:18033 DOID:4372 SNOMEDCT:75543006 RGO:18042 cerebral embolism RGO:18042 DOID:2426 ORDO:251937 RADLEX:RID4509 SNOMEDCT:128919000 RGO:18074 gangliocytoma RGO:18074 DOID:2384 RADLEX:RID5065 RGO:18089 Wernicke encephalopathy RGO:18089 RGO:18110 cerebellar mass in a child RGO:18110 RGO:18114 cerebellar mass in an adult RGO:18114 RADLEX:RID4221 SNOMEDCT:254965007 RGO:18126 pituitary macroadenoma RGO:18126 RGO:18159 CSF-intensity brainstem lesion RGO:18159 RGO:18162 CSF-intensity sellar/suprasellar lesion RGO:18162 RGO:18163 empty sella RGO:18163 RGO:18164 CSF-intensity posterior fossa lesion RGO:18164 Blake pouch mega-cisterna magna HP:0002280 SNOMEDCT:447739003 RGO:18166 mega cisterna magna RGO:18166 RADLEX:RID3337 RGO:18187 venous angioma RGO:18187 RGO:18234 intracranial MRI signal void RGO:18234 SNOMEDCT:70748002 RGO:18238 hemosiderin RGO:18238 RGO:18242 shunt tube RGO:18242 RGO:18245 dense intracranial calcification RGO:18245 RGO:18250 subependymal signal void RGO:18250 RGO:18253 parasellar signal void RGO:18253 RGO:18255 kissing carotids RGO:18255 RGO:18258 pneumatized posterior clinoid RGO:18258 RGO:18259 small ventricles and sulci RGO:18259 DOID:1573 HP:0001334 ICD10CM:G91.0 RADLEX:RID4886 SNOMEDCT:271569006 RGO:18266 communicating hydrocephalus RGO:18266 DOID:14159 ICD10CM:G91.1 RADLEX:RID4891 SNOMEDCT:230746009 RGO:18270 obstructive hydrocephalus RGO:18270 RGO:18277 asymmetrically enlarged lateral ventricles RGO:18277 cerebral hemiatrophy RADLEX:RID5149 SNOMEDCT:111337001 RGO:18278 Dyke-Davidoff-Masson syndrome RGO:18278 RGO:18284 large ventricles and sulci RGO:18284 RGO:18286 catabolic steroids RGO:18286 RGO:18288 abnormal ventricular configuration RGO:18288 RGO:18290 asymmetry of lateral ventricles RGO:18290 RGO:18298 CSF-intensity intraventricular mass RGO:18298 RGO:18321 intraventricular signal void RGO:18321 RGO:18332 CSF-intensity subarachnoid space lesion RGO:18332 RGO:18340 enhancing mass in cerebellopontine angle cistern RGO:18340 ICD10CM:I72.6 RGO:18342 aneurysm of vertebral artery RGO:18342 RGO:18345 nonenhancing mass in the cerebellopontine angle cistern RGO:18345 RGO:18346 focal leptomeningeal enhancement RGO:18346 RGO:18352 diffuse leptomeningeal enhancement RGO:18352 RGO:18358 nonenhancing pachymeningeal lesion RGO:18358 RGO:18361 pachymeningeal enhancement RGO:18361 RGO:18369 CSF-intensity extraaxial fluid collection RGO:18369 HP:0012444 RGO:18373 brain atrophy RGO:18373 RGO:18386 nonenhancing extraaxial mass RGO:18386 RGO:18389 enhancing extraaxial intracranial mass RGO:18389 angioblastic meningioma SNOMEDCT:277522009 RGO:18390 hemangiopericytoma of meninges RGO:18390 RGO:18391 metastasis to dura RGO:18391 RGO:18394 CSF-intensity extracranial mass RGO:18394 T1-dark extracranial mass RGO:18396 T1-hypointense extracranial mass RGO:18396 T1-bright extracranial mass RGO:18399 T1-hyperintense extracranial mass RGO:18399 RGO:18401 CSF-intensity intramedullary lesion RGO:18401 RGO:18402 posttraumatic cystic myelomalacia RGO:18402 RGO:18408 postinfarction RGO:18408 HP:0002171 RADLEX:RID3827 SNOMEDCT:81415000 RGO:18415 gliosis RGO:18415 RGO:18421 subacute infarction RGO:18421 RGO:18431 enhancing spinal cord lesion RGO:18431 Zuckerguss RGO:18432 leptomeningeal carcinomatosis RGO:18432 RGO:18434 diffusely small cord RGO:18434 RGO:18435 AIDS myelopathy RGO:18435 RADLEX:RID5046 SNOMEDCT:13331008 RGO:18436 atrophy RGO:18436 RGO:18437 collapsed syrinx RGO:18437 RGO:18438 cord tethering RGO:18438 RGO:18439 cord transection RGO:18439 RGO:18440 diffuse multiple sclerosis RGO:18440 RGO:18441 juvenile amyotrophy RGO:18441 HP:0002751 RADLEX:RID4760 RGO:18442 kyphoscoliosis RGO:18442 DOID:230 ICD10CM:G12.29 ORDO:35689 SNOMEDCT:81211007 RGO:18443 primary lateral sclerosis RGO:18443 RADLEX:RID5066 SNOMEDCT:36161006 RGO:18444 Wallerian degeneration RGO:18444 RGO:18445 focally small spinal cord RGO:18445 RGO:18446 bony spinal stenosis RGO:18446 RADLEX:RID39136 SNOMEDCT:33772003 RGO:18448 myelomalacia RGO:18448 RGO:18449 post infarction RGO:18449 DOID:11608 SNOMEDCT:24321005 RGO:18464 fungal meningitis RGO:18464 RGO:18465 postradiation vessel enlargement RGO:18465 RGO:18476 metastasis to subarachnoid space RGO:18476 DOID:0060058 HP:0002665 RADLEX:RID3840 SNOMEDCT:118600007 SNOMEDCT:21964009 RGO:18481 lymphoma RGO:18481 RGO:18485 extramedullary intradural signal void RGO:18485 RGO:18489 nerve root enhancement RGO:18489 DOID:12842 ICD10CM:G61.0 ORDO:2103 RADLEX:RID3465 SNOMEDCT:40956001 RGO:18492 Guillain-Barré syndrome RGO:18492 ORDO:329998 SNOMEDCT:426128009 RGO:18494 lymphomatous meningitis RGO:18494 RGO:18495 viral neuritis RGO:18495 RGO:18496 enlarged nerve roots RGO:18496 DOID:1803 HP:0031002 RADLEX:RID3505 SNOMEDCT:84299009 RGO:18498 neuritis RGO:18498 RGO:18499 toxic neuropathy RGO:18499 RGO:18500 extradural lesion with normal adjacent bone RGO:18500 RGO:18502 disk bulge RGO:18502 RGO:18503 disk extrusion RGO:18503 RGO:18504 disk protrusion RGO:18504 RADLEX:RID5079 SNOMEDCT:699330001 RGO:18505 marginal osteophyte RGO:18505 RGO:18509 conjoined root sleeve RGO:18509 DOID:11387 SNOMEDCT:61974008 RGO:18510 epidural abscess RGO:18510 HP:0100310 RADLEX:RID4708 SNOMEDCT:703861005 RGO:18512 epidural hematoma RGO:18512 SNOMEDCT:426399003 RGO:18513 epidural lipomatosis RGO:18513 RGO:18515 extruded or sequestered disk RGO:18515 RGO:18523 root sleeve diverticulum RGO:18523 RGO:18524 root sleeve ectasia RGO:18524 RGO:18525 facet joint synovial cyst RGO:18525 perineural cyst RADLEX:RID3932 SNOMEDCT:81634008 RGO:18526 Tarlov cyst RGO:18526 RGO:18528 extradural lesion with abnormal adjacent bone RGO:18528 RGO:18531 osseous metastasis with epidural soft tissue extension RGO:18531 RGO:18533 osteoporosis with fracture and granulation tissue RGO:18533 RGO:18540 granulocyte colony stimulating factor therapy RGO:18540 RGO:18552 T1-hyperintense diffuse vertebral body abnormality RGO:18552 DOID:12449 HP:0001915 SNOMEDCT:306058006 RGO:18553 aplastic anemia RGO:18553 RGO:18554 intermediate T1 intensity diffuse vertebral body abnormality RGO:18554 RGO:18559 T1-hypointense diffuse vertebral body abnormality RGO:18559 RGO:18561 globe lesion RGO:18561 DOID:5327 HP:0000541 RADLEX:RID4772 SNOMEDCT:42059000 RGO:18563 retinal detachment RGO:18563 HP:0007872 SNOMEDCT:255022003 RGO:18564 choroidal hemangioma RGO:18564 SNOMEDCT:416285004 RGO:18567 astrocytic hamartoma RGO:18567 DOID:4692 ORDO:199323 SNOMEDCT:1847009 RGO:18568 endophthalmitis RGO:18568 RGO:18569 glass prosthesis RGO:18569 RGO:18574 retrobulbar mass RGO:18574 RGO:18576 extraconal meningioma RGO:18576 neurilemoma neurinoma DOID:3192 HP:0100008 ORDO:252164 RADLEX:RID4473 SNOMEDCT:404022001 SNOMEDCT:985004 RGO:18578 schwannoma RGO:18578 RGO:18581 extraocular muscle enlargement RGO:18581 thyroid ophthalmopathy DOID:12361 HP:0100647 SNOMEDCT:353295004 RGO:18583 Graves disease RGO:18583 RGO:18584 venous obstruction RGO:18584 RGO:18589 lateral extraconal lesion RGO:18589 RGO:18595 enlarged superior ophthalmic vein RGO:18595 RGO:18596 orbital apex mass RGO:18596 RGO:18598 superior ophthalmic vein thrombosis RGO:18598 RGO:18599 infection of adjacent orbit RGO:18599 RGO:18602 orbital wall lesion RGO:18602 RGO:18604 meningioma with hyperostosis RGO:18604 SNOMEDCT:21708004 RGO:18605 osteoblastic osteosarcoma RGO:18605 RGO:18608 frontonasal encephalocele RGO:18608 RGO:18610 sinonasal mass without bone changes RGO:18610 RGO:18613 dried secretions RGO:18613 RGO:18616 sinolith RGO:18616 RGO:18617 undescended maxillary tooth RGO:18617 RGO:18618 sinonasal mass with bony remodeling without erosion RGO:18618 RGO:18619 pyomucocele RGO:18619 DOID:8538 RGO:18621 histiocytic lymphoma RGO:18621 RGO:18622 sinonasal mass with bony erosion RGO:18622 RGO:18627 extracranial meningioma RGO:18627 RGO:18629 vascular sinonasal mass with flow voids RGO:18629 RGO:18632 osseous paranasal sinus lesion RGO:18632 RGO:18633 skull base lesion RGO:18633 RGO:18638 squamous cell carcinoma extending through basal foramina RGO:18638 RADLEX:RID3537 RGO:18640 petrous apicitis RGO:18640 RGO:18643 salivary gland lesion RGO:18643 RGO:18646 intraparotid lymphadenopathy RGO:18646 RGO:18651 acute suppurative sialadenitis RGO:18651 RGO:18653 chronic recurrent sialadenitis RGO:18653 RGO:18654 chronic sialectasis RGO:18654 RGO:18655 lymphoepithelial sialadenopathy RGO:18655 DOID:12905 ICD10CM:K11.5 RADLEX:RID5010 SNOMEDCT:28826002 RGO:18657 sialolithiasis RGO:18657 Gougerot-Houwer-Sjögren syndrome Gougerot-Mikulicz-Sjögren syndrome Gougerot-Sjögren syndrome chronic autoimmune sialadenitis sicca syndrome DOID:12894 RGO:18658 Sjögren syndrome RGO:18658 DOID:1602 HP:0002840 ICD10CM:I88.1 RADLEX:RID3484 SNOMEDCT:19471005 RGO:18660 lymphadenitis RGO:18660 RGO:18661 neck mass RGO:18661 RGO:18667 colloid cyst of thyroid gland RGO:18667 RADLEX:RID4893 SNOMEDCT:40225001 SNOMEDCT:423984004 RGO:18668 hygroma RGO:18668 RGO:18672 tracheoesophageal cyst RGO:18672 RGO:18673 proton density-hyperintense supraspinatus tendon RGO:18673 RGO:18679 T2-hyperintense supraspinatus tendon RGO:18679 RGO:18696 absent bow-tie sign in knee meniscus RGO:18696 RGO:18697 bucket handle meniscal tear RGO:18697 RGO:18698 medial flipped flap tear RGO:18698 RGO:18699 radial meniscal tear RGO:18699 RGO:18702 regional migratory osteoporosis RGO:18702 RGO:18706 posttraumatic osteonecrosis RGO:18706 RGO:18712 T2-hypointense intra-articular knee mass RGO:18712 RGO:18714 infrapatellar mass in Hoffa fat pad RGO:18714 RGO:18715 chronic lateral ankle pain RGO:18715 RGO:18716 anterolateral ankle impingement RGO:18716 RGO:18717 lateral ligament tear RGO:18717 RGO:18718 longitudinal split tear of peroneus brevis RGO:18718 SNOMEDCT:444878001 RGO:18719 sinus tarsi syndrome RGO:18719 RGO:18720 T2-hyperintense liver lesion RGO:18720 HP:0025519 SNOMEDCT:27721004 RGO:18731 biliary hamartoma RGO:18731 RGO:18733 ciliated hepatic foregut cyst RGO:18733 RADLEX:RID3988 SNOMEDCT:403980002 SNOMEDCT:66229009 RGO:18734 hemangioendothelioma RGO:18734 RGO:18740 T1-hyperintense liver lesion RGO:18740 RGO:18741 focal fatty infiltration RGO:18741 T2-dark liver lesion RGO:18748 T2-hypointense liver lesion RGO:18748 RADLEX:RID39157 SNOMEDCT:413643004 SNOMEDCT:74947009 RGO:18750 gas RGO:18750 RGO:18758 arterial hyperenhancement of focal liver lesion RGO:18758 RGO:18777 peribiliary cyst RGO:18777 RGO:18791 compression or obstruction of portal vein by lymphadenopathy or mass RGO:18791 hypercoagulability SNOMEDCT:76612001 RGO:18792 hypercoagulable state RGO:18792 RGO:18793 inflammation secondary to pancreatitis, appendicitis, diverticulitis RGO:18793 RGO:18794 T2-hyperintense periportal tissue RGO:18794 RGO:18795 bile leak RGO:18795 liver transplantation RGO:18799 liver transplant RGO:18799 RGO:18806 mass in the porta hepatis RGO:18806 RGO:18814 ampullary stenosis RGO:18814 RGO:18825 biliary tract filling defect RGO:18825 RADLEX:RID5598 SNOMEDCT:65818007 RGO:18829 stent RGO:18829 RGO:18832 T2-hypointense intraluminal gallbladder lesion RGO:18832 RGO:18834 iodinated contrast RGO:18834 RGO:18837 T2-hyperintense intraluminal gallbladder lesion RGO:18837 RGO:18841 T1-hyperintense intraluminal gallbladder lesion RGO:18841 RGO:18842 mass in inferior vena cava RGO:18842 RGO:18847 T2-hyperintense adrenal mass RGO:18847 RGO:18852 T2-intermediate adrenal mass RGO:18852 T1-bright adrenal mass RGO:18855 T1-hyperintense adrenal mass RGO:18855 RGO:18859 T2-intermediate renal mass RGO:18859 T2-bright renal mass RGO:18863 T2-hyperintense renal mass RGO:18863 RGO:18864 acquired cystic disease of dialysis RGO:18864 RGO:18868 renal vein thrombus RGO:18868 T2-dark renal mass RGO:18869 T2-hypointense renal mass RGO:18869 RGO:18871 leukemic infiltrate RGO:18871 T1-bright renal mass RGO:18872 T1-hyperintense renal mass RGO:18872 RGO:18876 T2-hyperintense endometrial uterine mass RGO:18876 polyp of endometrium SNOMEDCT:11314008 RGO:18877 endometrial polyp RGO:18877 SNOMEDCT:65727000 RGO:18879 intrauterine pregnancy RGO:18879 RGO:18881 tamoxifen changes RGO:18881 RGO:18883 T2-intermediate endometrial uterine mass RGO:18883 T2-dark endometrial uterine mass RGO:18885 T2-hypointense endometrial uterine mass RGO:18885 ORDO:180126 SNOMEDCT:22504001 RGO:18889 septate uterus RGO:18889 T1-bright endometrial uterine mass RGO:18890 T1-hyperintense endometrial uterine mass RGO:18890 RGO:18892 gestational trophoblastic disease with hemorrhage RGO:18892 RGO:18894 retained products of conception with hemorrhage RGO:18894 T2-bright myometrial uterine mass RGO:18897 T2-hyperintense myometrial uterine mass RGO:18897 SNOMEDCT:4316006 RGO:18900 myometritis RGO:18900 RADLEX:RID39545 RGO:18902 vessels RGO:18902 RGO:18904 T2-intermediate myometrial uterine mass RGO:18904 RGO:18908 T2-hypointense myometrial uterine mass RGO:18908 RGO:18912 T1-hyperintense myometrial uterine mass RGO:18912 RGO:18914 leiomyoma with hemorrhage RGO:18914 DOID:4386 RADLEX:RID4389 SNOMEDCT:430750000 SNOMEDCT:44598004 RGO:18915 lipoleiomyoma RGO:18915 T2-bright adnexal mass RGO:18917 T2-hyperintense adnexal mass RGO:18917 RGO:18918 clear cell adenocarcinoma of ovary RGO:18918 DOID:2871 SNOMEDCT:30289006 RGO:18920 endometrioid carcinoma RGO:18920 torsion of ovary SNOMEDCT:13595002 RGO:18925 ovarian torsion RGO:18925 SNOMEDCT:276870001 RGO:18928 carcinoma of fallopian tube RGO:18928 ICD10CM:N83.6 SNOMEDCT:78095005 RGO:18930 hematosalpinx RGO:18930 DOID:2640 SNOMEDCT:24327009 RGO:18931 struma ovarii RGO:18931 T2-dark adnexal mass RGO:18932 T2-hypointense adnexal mass RGO:18932 ovarian fibrothecoma ORDO:314478 RADLEX:RID4562 SNOMEDCT:52490000 RGO:18934 fibrothecoma RGO:18934 T1-bright adnexal mass RGO:18938 T1-hyperintense adnexal mass RGO:18938 RGO:18940 ectopic pregnancy with hemorrhage RGO:18940 RGO:18942 ovarian torsion with hemorrhage RGO:18942 T2-bright prostate mass RGO:18945 T2-hyperintense prostate mass RGO:18945 T2-dark prostate mass RGO:18950 T2-hypointense prostate mass RGO:18950 RGO:18951 intraglandular dysplasia RGO:18951 T1-bright prostate mass RGO:18953 T1-hyperintense prostate mass RGO:18953 RGO:18966 cervical teratoma RGO:18966 RGO:18986 large fetus for dates RGO:18986 RGO:18987 inaccurate dates RGO:18987 ICD10CM:O30 RGO:18988 multiple gestation RGO:18988 RGO:18989 maternal obesity RGO:18989 RGO:18990 small fetus for dates RGO:18990 DOID:302 SNOMEDCT:66214007 RGO:18995 substance abuse RGO:18995 RGO:18996 cyanotic cardiopulmonary disease RGO:18996 IUGR HP:0001511 SNOMEDCT:22033007 RGO:18998 intrauterine growth retardation RGO:18998 RGO:18999 chorioangioma of placenta RGO:18999 RGO:19000 congenital malformation or syndrome RGO:19000 twin transfusion syndrome DOID:13576 ORDO:95431 RGO:19003 twin-to-twin transfusion syndrome RGO:19003 RGO:19008 failure of fetal head to engage during labor RGO:19008 RGO:19011 low-lying placenta RGO:19011 SNOMEDCT:199397009 RGO:19014 cephalopelvic disproportion RGO:19014 RGO:19019 fetal cranial deformity RGO:19019 HP:0011815 SNOMEDCT:55999004 RGO:19020 cephalocele RGO:19020 HP:0030769 SNOMEDCT:84461004 RGO:19021 exencephaly RGO:19021 dead fetus RGO:19022 fetal demise RGO:19022 RGO:19023 open neural tube defect RGO:19023 midline cystic fetal brain mass RGO:19025 midline cystic mass in fetal brain RGO:19025 RGO:19027 asymmetrical cystic mass in fetal brain RGO:19027 HP:0002170 SNOMEDCT:1386000 RGO:19030 intracranial hemorrhage RGO:19030 RGO:19034 nasal-facial-digital syndrome RGO:19034 RGO:19036 posthemorrhagic RGO:19036 RGO:19037 postinflammatory RGO:19037 RGO:19038 large fetal intracranial fluid collection RGO:19038 HP:0006988 ORDO:93925 RADLEX:RID34734 SNOMEDCT:253137003 RGO:19039 alobar holoprosencephaly RGO:19039 RGO:19040 massive hydrocephalus RGO:19040 RGO:19041 fetal intracranial calcification RGO:19041 RGO:19042 cytomegalovirus infection in utero RGO:19042 RGO:19043 herpes simplex type II infection in utero RGO:19043 RGO:19044 toxoplasmosis infection in utero RGO:19044 RGO:19046 straight fetal spine RGO:19046 ICD10CM:O00.0 SNOMEDCT:82661006 RGO:19047 abdominal pregnancy RGO:19047 HP:0001623 SNOMEDCT:6096002 RGO:19048 breech presentation RGO:19048 RGO:19053 fetal neck mass RGO:19053 HP:0012498 SNOMEDCT:302929008 RGO:19055 nuchal cord RGO:19055 RGO:19060 twin sac of blighted ovum RGO:19060 RGO:19061 fetal chest mass RGO:19061 ICD10CM:J94.8 SNOMEDCT:79231000 RGO:19062 hydrothorax RGO:19062 HP:0009730 RADLEX:RID4395 SNOMEDCT:302846007 SNOMEDCT:43375002 RGO:19063 rhabdomyoma RGO:19063 RGO:19064 fetal cardiac mass RGO:19064 RGO:19065 aneurysm of foramen ovale RGO:19065 RGO:19066 thickening of chordae tendineae RGO:19066 RGO:19067 nonvisualization of fetal stomach RGO:19067 RGO:19068 CNS disorder RGO:19068 DOID:12215 HP:0001562 ICD10CM:O41.0 SNOMEDCT:59566000 RGO:19070 oligohydramnios RGO:19070 HP:0002006 RGO:19071 facial cleft RGO:19071 RGO:19074 normal variant in 2nd trimester RGO:19074 RGO:19075 blood in amniotic fluid RGO:19075 RGO:19077 fetal hepatosplenomegaly RGO:19077 SNOMEDCT:462166006 RGO:19079 fetal anemia RGO:19079 RGO:19081 cystic fetal abdominal mass RGO:19081 RGO:19084 meconium pseudocyst RGO:19084 RGO:19085 megacystic-microcolon-hypoperistalsis syndrome RGO:19085 HP:0030656 RGO:19087 umbilical vein varix RGO:19087 RGO:19088 cystic fetal upper abdominal mass RGO:19088 RGO:19091 cystic fetal mid-abdominal mass RGO:19091 RGO:19094 cystic fetal pelvic mass RGO:19094 RGO:19095 fetal intra-abdominal calcification RGO:19095 RGO:19098 large fetal abdomen during third trimester RGO:19098 HP:0000113 RGO:19102 polycystic kidneys RGO:19102 HP:0001791 SNOMEDCT:363125002 RGO:19106 fetal ascites RGO:19106 DOID:4175 RGO:19112 Rh isoimmunization RGO:19112 RGO:19115 fetal anterior abdominal wall defect RGO:19115 DOID:11044 HP:0001543 ICD10CM:Q79.3 ORDO:2368 SNOMEDCT:72951007 RGO:19116 gastroschisis RGO:19116 HP:0030754 SNOMEDCT:17234001 RGO:19119 allantoic cyst RGO:19119 ORDO:93929 SNOMEDCT:20815007 RGO:19120 exstrophy of cloaca RGO:19120 RGO:19121 fetal skin thickening RGO:19121 DOID:4027 HP:0025116 SNOMEDCT:130955003 RGO:19123 fetal distress RGO:19123 HP:0010957 RGO:19127 posterior urethral valves RGO:19127 HP:0001788 ICD10CM:O42 SNOMEDCT:44223004 RGO:19128 premature rupture of membranes RGO:19128 caudal dysplasia sequence ORDO:3027 SNOMEDCT:8301004 RGO:19130 caudal regression syndrome RGO:19130 RGO:19131 cytogenetic-triploidy syndrome RGO:19131 RGO:19132 impending fetal death RGO:19132 RGO:19135 urethral agenesis RGO:19135 DOID:8488 HP:0001561 ICD10CM:O40 SNOMEDCT:86203003 RGO:19136 polyhydramnios RGO:19136 SNOMEDCT:204052006 RGO:19137 cebocephaly RGO:19137 RGO:19141 coarctation or interruption of fetal aorta RGO:19141 RGO:19144 twin-twin transfusion in monochorionic twins RGO:19144 DOID:0060646 ORDO:264688 SNOMEDCT:233646003 RGO:19146 congenital chylothorax RGO:19146 RADLEX:RID39322 RGO:19147 fetal hydrops RGO:19147 RGO:19152 Rh incompatibility RGO:19152 RGO:19153 thin placenta RGO:19153 RGO:19155 thickened placenta RGO:19155 RGO:19157 maternal diabetes mellitus RGO:19157 RGO:19159 congenital fetal anomaly RGO:19159 RGO:19160 maternal heart failure RGO:19160 RGO:19162 placental hemorrhage RGO:19162 RGO:19164 solid placental mass RGO:19164 RGO:19166 hypoechoic placental lesion RGO:19166 SNOMEDCT:80256005 RGO:19168 intervillous thrombosis RGO:19168 RGO:19169 maternal lake RGO:19169 RGO:19170 mature placenta RGO:19170 RGO:19171 normal subplacental complex RGO:19171 RGO:19172 septal cyst RGO:19172 RGO:19173 subchorionic lake RGO:19173 DOID:277 SNOMEDCT:2099007 SNOMEDCT:237268002 SNOMEDCT:699948001 RGO:19174 chorioangioma RGO:19174 ICD10CM:O43.11 SNOMEDCT:2437000 RGO:19175 circumvallate placenta RGO:19175 RGO:19176 perivillous or subchorionic fibrin deposition RGO:19176 RGO:19177 subchorionic thrombosis RGO:19177 RGO:19178 retroplacental mass RGO:19178 SNOMEDCT:237293000 RGO:19180 retroplacental hematoma RGO:19180 RGO:19181 submembranous hematoma RGO:19181 RGO:19182 umbilical cord enlargement RGO:19182 RGO:19184 knotted umbilical cord RGO:19184 RGO:19185 localized deposition of Wharton jelly RGO:19185 RGO:19186 thrombosis of umbilical vessels RGO:19186 RGO:19187 umbilical cord angioma RGO:19187 HP:0030654 RGO:19188 umbilical cord cyst RGO:19188 RGO:19189 umbilical artery aneurysm RGO:19189 RGO:19190 early intrauterine pregnancy RGO:19190 RGO:19191 double decidual sign RGO:19191 RGO:19192 fetal pole within uterine cavity RGO:19192 RGO:19193 gestational sac with yolk sac within endometrial cavity RGO:19193 RGO:19194 intradecidual sign RGO:19194 RGO:19195 endometrial fluid and positive beta-hCG RGO:19195 RGO:19196 decidual cyst RGO:19196 RGO:19199 ovarian mass in pregnancy RGO:19199 RGO:19201 malignant ovarian neoplasm RGO:19201 torsion of testicle DOID:11996 HP:0100813 SNOMEDCT:81996005 RGO:19207 testicular torsion RGO:19207 APVC APVR anomalous pulmonary venous connection HP:0010772 ORDO:3090 RGO:19209 anomalous pulmonary venous return RGO:19209 distal phalangeal erosion erosion of terminal phalangeal tuft DOID:0050525 HP:0009771 RGO:19217 acro-osteolysis RGO:19217 DOID:1532 RGO:19224 pleural disease RGO:19224 DOID:0060227 ORDO:974 SNOMEDCT:34748004 RGO:19230 Adams-Oliver syndrome RGO:19230 Smith-McCort dysplasia RGO:19243 Smith-McCort syndrome RGO:19243 Saldino-Mainzer dysplasia acrodysplasia with retinitis pigmentosa and nephropathy ORDO:140969 RGO:19246 Saldino-Mainzer syndrome RGO:19246 Mau-Nilsonne syndrome tibia vara DOID:14798 ORDO:2768 RADLEX:RID29059 RGO:19247 Blount disease RGO:19247 SNOMEDCT:47381006 RGO:19248 saber shin RGO:19248 Caffey disease including infantile and attenuated forms Caffey-Silverman syndrome Caffey-Smyth disease Röske-de Toni-Caffey-Smyth disease de Toni-Caffey disease infantile cortical hyperostosis DOID:4257 ORDO:1310 RADLEX:RID29063 SNOMEDCT:24752008 RGO:19251 Caffey disease RGO:19251 tubular stenosis dysplasia ORDO:2333 SNOMEDCT:82837002 RGO:19257 Kenny-Caffey syndrome RGO:19257 ADAM complex Streeter bands amniotic band constriction amniotic band sequence ORDO:1034 SNOMEDCT:440214006 RGO:19263 amniotic band syndrome RGO:19263 RGO:19271 familial callus formation RGO:19271 bone islands enostosis RADLEX:RID4003 SNOMEDCT:25994006 RGO:19280 bone island RGO:19280 RGO:19281 periapical idiopathic osteosclerosis RGO:19281 DOID:0050591 HP:0000668 ICD10CM:K00.0 SNOMEDCT:64969001 RGO:19284 hypodontia RGO:19284 HP:0000689 SNOMEDCT:47944004 SNOMEDCT:707598004 RGO:19285 malocclusion RGO:19285 DOID:1930 ORDO:2377 SNOMEDCT:232059000 RGO:19288 Laurence-Moon syndrome RGO:19288 RADLEX:RID35343 SNOMEDCT:16442005 RGO:19290 leontiasis ossea RGO:19290 HP:0011967 ICD10CM:E61.0 SNOMEDCT:19577007 RGO:19296 copper deficiency RGO:19296 triple X syndrome trisomy X SNOMEDCT:35111009 RGO:19300 XXX syndrome RGO:19300 DOID:4590 SNOMEDCT:40935003 RGO:19308 meningiomatosis RGO:19308 bilateral acoustic neuroma bilateral vestibular schwannoma RGO:19309 bilateral acoustic schwannomas RGO:19309 RGO:19310 bilateral optic nerve gliomas RGO:19310 RGO:19311 cerebral gliomas RGO:19311 RGO:19312 choroid plexus papillomas RGO:19312 RGO:19313 multiple spine tumors RGO:19313 RGO:19314 multiple spine arteriovenous malformations RGO:19314 RGO:19317 retinal angiomatosis RGO:19317 RGO:19318 subependymal tuber RGO:19318 RGO:19319 intraventricular glioma RGO:19319 RGO:19320 giant cell astrocytoma RGO:19320 RGO:19323 intracerebral hemangioma RGO:19323 RGO:19324 intracerebral arteriovenous malformation RGO:19324 RGO:19325 cutaneous hemangioma RGO:19325 RGO:19326 cutaneous arteriovenous malformation RGO:19326 RGO:19329 chemical acro-osteolysis RGO:19329 HP:0006482 RGO:19331 malformed teeth RGO:19331 RGO:19332 defective teeth RGO:19332 RGO:19340 prolonged steroid therapy RGO:19340 RGO:19343 idiopathic osteonecrosis RGO:19343 RADLEX:RID4770 SNOMEDCT:87642003 RGO:19345 dislocation RGO:19345 RGO:19346 surgical correction of congenital hip dysplasia RGO:19346 RGO:19347 hip nailing RGO:19347 SNOMEDCT:110398004 RGO:19348 microfracture RGO:19348 ICD10CM:M00 SNOMEDCT:372939007 RGO:19350 pyogenic arthritis RGO:19350 RGO:19353 avascular necrosis of phalanges RGO:19353 RGO:19356 widespread reflex sympathetic dystrophy RGO:19356 DOID:12603 HP:0002488 SNOMEDCT:24072005 SNOMEDCT:91855006 RGO:19359 acute leukemia RGO:19359 RGO:19360 severe iron deficiency RGO:19360 DOID:14717 SNOMEDCT:82077006 RGO:19363 myotubular myopathy RGO:19363 RGO:19367 Pena-Shokeir syndrome RGO:19367 G syndrome Opitz G/BBB syndrome hypertelorism-hypospadias syndrome hypospadias-hypertelorism syndrome ORDO:2745 RGO:19378 Opitz BBBG syndrome RGO:19378 Pierre Robin syndrome HP:0000201 SNOMEDCT:4602007 RGO:19390 Robin sequence RGO:19390 RGO:19398 chronic subdural hematoma RGO:19398 fractures RADLEX:RID4650 SNOMEDCT:125605004 SNOMEDCT:72704001 RGO:19412 fracture RGO:19412 RGO:19415 chronic hypervitaminosis A RGO:19415 RGO:19416 neonatal hyperthyroidism RGO:19416 Salter-Harris fracture RGO:19417 epiphyseal-metaphyseal fracture RGO:19417 SNOMEDCT:254092004 RGO:19419 conorenal syndrome RGO:19419 RGO:19423 trauma to cartilage RGO:19423 RGO:19424 epiphyseal-metaphyseal injury RGO:19424 SNOMEDCT:254119005 RGO:19425 neonatal hyperparathyroidism RGO:19425 RGO:19426 immune deficiency syndromes RGO:19426 RGO:19427 metaphyseal dysplasia with thymolymphopenia RGO:19427 SNOMEDCT:89454001 RGO:19428 Schwachman-Diamond syndrome RGO:19428 RGO:19429 treated leukemia RGO:19429 RGO:19430 idiopathic sclerosis RGO:19430 RGO:19435 peritendinitis calcarea RGO:19435 RGO:19436 kikuya bursa RGO:19436 RADLEX:RID49919 SNOMEDCT:422411000 SNOMEDCT:63130001 RGO:19437 surgical scar RGO:19437 RGO:19439 soft tissue osteosarcoma RGO:19439 juxtacortical osteosarcoma DOID:3373 RADLEX:RID4021 SNOMEDCT:128918008 RGO:19440 parosteal osteosarcoma RGO:19440 RADLEX:RID5229 SNOMEDCT:298285004 RGO:19441 acrosclerosis RGO:19441 RGO:19442 gas phlegmon RGO:19442 DOID:9159 ICD10CM:A48.0 SNOMEDCT:80466000 RGO:19443 gas gangrene RGO:19443 HP:0001907 SNOMEDCT:371039008 RGO:19446 thromboembolic disease RGO:19446 RGO:19448 electroshock RGO:19448 RGO:19450 soft tissue infection adjacent to bone RGO:19450 ICD10CM:W50.3 SNOMEDCT:242605002 SNOMEDCT:43028005 RGO:19451 human bite RGO:19451 SNOMEDCT:31986002 RGO:19452 animal bite RGO:19452 RADLEX:RID34715 SNOMEDCT:19514005 RGO:19459 arthritis mutilans RGO:19459 RGO:19460 bound feet RGO:19460 sickle cell dactylitis RGO:19461 hand-foot syndrome RGO:19461 RGO:19462 severe osteomyelitis RGO:19462 SNOMEDCT:12143007 RGO:19465 developmental cyst RGO:19465 DOID:3149 HP:0031525 SNOMEDCT:254662007 RGO:19467 keratoacanthoma RGO:19467 SNOMEDCT:403410004 RGO:19468 multicentric infantile myofibromatosis RGO:19468 osteonecrosis of lunate osteonecrosis of the carpal lunate ORDO:97332 RADLEX:RID5182 RGO:19469 Kienböck disease RGO:19469 SNOMEDCT:8664001 RGO:19473 myxofibroma RGO:19473 RGO:19474 healing nonossifying fibroma RGO:19474 RGO:19478 chronic lead poisoning RGO:19478 RGO:19481 nutritional copper deficiency RGO:19481 severe acute respiratory syndrome DOID:2945 SNOMEDCT:398447004 SNOMEDCT:415360003 RGO:19484 SARS RGO:19484 HP:0000824 SNOMEDCT:397827003 RGO:19485 growth hormone deficiency RGO:19485 postinflammatory or posttraumatic cerebral degeneration RGO:19486 contracting skull RGO:19486 DOID:0060873 SNOMEDCT:237837007 RGO:19489 primordial dwarfism RGO:19489 RGO:19490 intrasellar subarachnoid cyst RGO:19490 RGO:19491 subarachnoid cyst RGO:19491 RGO:19493 optic chiasm neurofibroma RGO:19493 RGO:19502 osteofibrous dysplasia RGO:19502 RGO:19504 benign tropical ulcer RGO:19504 DOID:6610 RGO:19505 bone hemangioma RGO:19505 RGO:19506 cystic type lymphangioma RGO:19506 RGO:19508 subungual keratoma RGO:19508 DOID:13523 ICD10CM:B74.3 ORDO:2404 SNOMEDCT:44250009 RGO:19515 loiasis RGO:19515 SNOMEDCT:47759003 RGO:19516 Loa loa RGO:19516 DOID:4976 SNOMEDCT:240820001 RGO:19517 elephantiasis RGO:19517 familial sensory neural radiculopathy RGO:19519 Hicks syndrome RGO:19519 RGO:19521 myocardial abnormality RGO:19521 SNOMEDCT:698247007 RGO:19522 cardiac dysrhythmia RGO:19522 RGO:19523 unilateral hydrocephalus RGO:19523 body stalk anomaly RGO:19529 limb-body wall complex RGO:19529 HP:0030716 ICD10CM:Q00.0 SNOMEDCT:203923004 RGO:19531 acrania RGO:19531 RGO:19532 cranial dysplasia RGO:19532 avascular necrosis of the inferior ossification center of the patella osteonecrosis of the secondary patellar ossification center RGO:19534 Sinding-Larsen disease RGO:19534 RGO:19537 abnormal position of patella RGO:19537 RGO:19540 bone dysplasia RGO:19540 RGO:19541 paresis of quadriceps muscle RGO:19541 HP:0003982 RGO:19543 absent ulna RGO:19543 RGO:19545 hypoplasia or aplasia of ulna RGO:19545 RGO:19546 hypoplasia or aplasia of fourth and fifth fingers RGO:19546 HME MHE diaphyseal aclasis multiple cartilaginous exostoses multiple hereditary exostoses multiple osteochondromas multiple osteochondromatosis osteochondromatosis DOID:206 RADLEX:RID4137 RGO:19547 hereditary multiple exostoses RGO:19547 RGO:19550 congenital thumb abnormality RGO:19550 HP:0009829 SNOMEDCT:22841008 RGO:19551 phocomelia RGO:19551 RGO:19554 familial brachydactyly D RGO:19554 SNOMEDCT:197928006 RGO:19560 chronic urinary tract infection RGO:19560 UTI SNOMEDCT:68566005 RGO:19561 urinary tract infection RGO:19561 HP:0100281 SNOMEDCT:54597004 RGO:19563 chronic colitis RGO:19563 RGO:19568 early enchondromatosis RGO:19568 RGO:19571 healing scurvy RGO:19571 SNOMEDCT:191268006 RGO:19572 chronic anemia RGO:19572 RGO:19574 biliary rickets RGO:19574 RGO:19576 severe pseudoachondroplasia RGO:19576 RGO:19577 severe hyperparathyroidism RGO:19577 SNOMEDCT:70528007 RGO:19579 mucolipidosis RGO:19579 RADLEX:RID35314 RGO:19582 ivory osteoma RGO:19582 DOID:0050853 SNOMEDCT:20696009 RGO:19583 chronic venous insufficiency RGO:19583 RGO:19584 chronic arterial insufficiency RGO:19584 RGO:19585 chronic lymphatic insufficiency RGO:19585 RGO:19586 prostaglandin E RGO:19586 RGO:19588 pancreatitis with bone lesions RGO:19588 RGO:19589 physiologic periostitis of newborn RGO:19589 RGO:19590 diffuse osteomyelitis RGO:19590 RGO:19592 cystic type lymphangiomatosis RGO:19592 HP:0001250 RADLEX:RID28806 SNOMEDCT:91175000 RGO:19593 seizure RGO:19593 electric shock therapy SNOMEDCT:23835007 RGO:19594 electroconvulsive therapy RGO:19594 RGO:19600 severe inflammatory periostitis RGO:19600 RGO:19602 idiopathic pectus carinatum RGO:19602 RGO:19603 idiopathic rib notching RGO:19603 DOID:12835 HP:0002445 ICD10CM:G82.5 SNOMEDCT:11538006 RGO:19604 quadriplegia RGO:19604 innominate vein obstruction RGO:19605 obstruction of innominate vein RGO:19605 subclavian vein obstruction RGO:19606 obstruction of subclavian vein RGO:19606 RGO:19609 intercostal neurofibroma RGO:19609 RGO:19610 intercostal neurilemoma RGO:19610 RGO:19613 advanced arteriosclerosis RGO:19613 RGO:19614 aortic thrombosis RGO:19614 RGO:19617 pulmonary valvular atresia RGO:19617 RGO:19618 idiopathic pectus excavatum RGO:19618 Hurler-Scheie syndrome MPS 1 H-S RGO:19632 mucopolysaccharidosis type 1 H-S RGO:19632 SNOMEDCT:307816004 RGO:19647 Leriche syndrome RGO:19647 DOID:13375 ORDO:397 RADLEX:RID3686 SNOMEDCT:414341000 RGO:19648 giant cell arteritis RGO:19648 RGO:19649 Butazolidin RGO:19649 RGO:19651 immunosuppressive drug RGO:19651 RGO:19652 cytotoxic therapy RGO:19652 RGO:19653 Indocin RGO:19653 DOID:0080037 SNOMEDCT:254131007 RGO:19654 autosomal dominant osteosclerosis RGO:19654 RGO:19658 stippled calcaneus RGO:19658 fungus ball ICD10CM:B47 ORDO:2583 RADLEX:RID28507 SNOMEDCT:410039003 RGO:19659 mycetoma RGO:19659 HP:0008127 RGO:19660 bipartite calcaneus RGO:19660 DOID:13189 HP:0001997 SNOMEDCT:48440001 RGO:19661 gouty arthritis RGO:19661 RGO:19662 vascular stasis RGO:19662 RGO:19663 idiopathic pseudoarthrosis RGO:19663 RGO:19664 familial pseudoarthrosis RGO:19664 RGO:19667 Milkman syndrome RGO:19667 RGO:19668 metaphyseal chip fractures RGO:19668 RGO:19669 bifid rib RGO:19669 RGO:19671 rib synostosis RGO:19671 oligosaccharidosis RGO:19683 glycoprotein storage disease RGO:19683 RGO:19685 fucosidosis type 1 RGO:19685 RGO:19686 fucosidosis type 2 RGO:19686 RGO:19687 angiomatous bone lesion RGO:19687 H-shaped vertebra Lincoln log vertebra RGO:19693 step-like vertebra RGO:19693 SNOMEDCT:18040001 RGO:19695 senile osteoporosis RGO:19695 SNOMEDCT:102447009 RGO:19696 postmenopausal osteoporosis RGO:19696 ICD10CM:E61.1 SNOMEDCT:35240004 RGO:19697 iron deficiency RGO:19697 RGO:19698 chronic hyperflexion of spine RGO:19698 HP:0001252 RGO:19699 muscular hypotonia RGO:19699 RGO:19700 normal variant spine RGO:19700 long fingers DOID:0050455 HP:0001166 SNOMEDCT:62250003 RGO:19701 arachnodactyly RGO:19701 RGO:19703 other narrow thorax-short rib syndromes RGO:19703 Fiessinger-Leroy disease Fiessinger-Leroy-Reiter syndrome Reiter arthritis arthritis urethritica polyarteritis enterica post-infectious arthritis reactive arthritis venereal arthritis RADLEX:RID3562 RGO:19706 Reiter syndrome RGO:19706 SNOMEDCT:202391009 RGO:19709 chronic joint effusion RGO:19709 RGO:19710 idiopathic popliteal cyst RGO:19710 SNOMEDCT:372247004 RGO:19711 fungal arthritis RGO:19711 HP:0010048 RGO:19713 absent metacarpals RGO:19713 RGO:19716 normal in young infants RGO:19716 RGO:19717 idiopathic Wormian bones RGO:19717 RGO:19718 primary craniosynostosis RGO:19718 RGO:19719 chronic increased intracranial pressure RGO:19719 RGO:19721 collateral cerebral circulation RGO:19721 venous sinus thrombosis RGO:19722 thrombosis of venous sinus RGO:19722 ICA occlusion internal carotid artery occlusion occlusion of ICA SNOMEDCT:433821000124102 RGO:19723 occlusion of internal carotid artery RGO:19723 DOID:589 HP:0004804 SNOMEDCT:42601008 RGO:19729 congenital hemolytic anemia RGO:19729 HP:0004445 ORDO:288 SNOMEDCT:250242004 RGO:19730 elliptocytosis RGO:19730 DOID:1341 SNOMEDCT:63565007 RGO:19731 congenital anemia RGO:19731 RGO:19733 severe iron deficiency anemia RGO:19733 carcinoma of prostate prostate cancer DOID:10286 SNOMEDCT:254900004 RGO:19737 prostate carcinoma RGO:19737 SNOMEDCT:13141002 RGO:19739 calcinosis circumscripta RGO:19739 RGO:19741 coal-worker pneumoconiosis RGO:19741 RGO:19748 ruptured popliteal cyst RGO:19748 noninfectious synovitis RGO:19749 noninfective synovitis RGO:19749 SNOMEDCT:57451009 RGO:19755 Mounier-Kuhn syndrome RGO:19755 DOID:2583 HP:0004432 SNOMEDCT:119249001 RGO:19756 agammaglobulinemia RGO:19756 A1AD A1AT deficiency AAT deficiency alpha 1-antitrypsin deficiency alpha-1 alpha-1 antitrypsin deficiency RGO:19757 alpha1-antitrypsin deficiency RGO:19757 DOID:6132 HP:0012387 RADLEX:RID34637 SNOMEDCT:32398004 RGO:19758 bronchitis RGO:19758 RGO:19762 thoracic drainage tube RGO:19762 RGO:19763 rib retractor RGO:19763 healed or healing fracture ICD10CM:L84 SNOMEDCT:201040000 RGO:19764 callus RGO:19764 ICD10CM:A18.03 SNOMEDCT:58764007 RGO:19765 tuberculous osteomyelitis RGO:19765 RGO:19766 syphilitic osteomyelitis RGO:19766 RGO:19767 fungal osteomyelitis RGO:19767 RGO:19770 fused rib RGO:19770 RGO:19775 severe osteoporosis RGO:19775 DOID:0110340 ORDO:216820 RGO:19777 osteogenesis imperfecta type 4 RGO:19777 RGO:19778 malunited fracture of femoral neck RGO:19778 RGO:19779 epiphyseal-physeal-metaphyseal fracture RGO:19779 RGO:19780 poor nutrition RGO:19780 RGO:19781 rapid growth spurt RGO:19781 RGO:19782 growth hormone deficiency and therapy RGO:19782 RGO:19785 chorionic gonadotropin therapy RGO:19785 SNOMEDCT:285655001 RGO:19787 mechanical stress RGO:19787 RGO:19788 fracture nonunion with secondary deformity RGO:19788 RGO:19789 limb hypertrophy RGO:19789 RGO:19790 epiphyseal injury RGO:19790 RGO:19791 malunited fracture RGO:19791 bilateral hereditary microepiphyseal dysplasia RGO:19792 Elsbach dysplasia RGO:19792 RGO:19795 fracture of femoral neck RGO:19795 RGO:19796 surgical or manipulative trauma RGO:19796 RGO:19798 overgrowth of fibula RGO:19798 RGO:19802 bleeding disorder with chronic hemarthrosis RGO:19802 SNOMEDCT:314214009 RGO:19803 chronic osteomyelitis of tibia RGO:19803 SNOMEDCT:40970001 RGO:19805 chronic osteomyelitis RGO:19805 RGO:19807 polychondritis RGO:19807 RGO:19809 mitral valve repair RGO:19809 SNOMEDCT:1770009 RGO:19810 mitral valvotomy RGO:19810 RGO:19811 balloon valvoplasty RGO:19811 RGO:19812 dysfunctional prosthetic mitral valve RGO:19812 DOID:13725 ICD10CM:E51.1 SNOMEDCT:36656008 RGO:19813 beriberi RGO:19813 HP:0011105 SNOMEDCT:21639008 RGO:19815 hypervolemia RGO:19815 SNOMEDCT:35633007 RGO:19817 overtransfusion RGO:19817 HP:0001945 SNOMEDCT:386661006 RGO:19818 pyrexia RGO:19818 SNOMEDCT:76571007 RGO:19819 septic shock RGO:19819 HP:0006554 ORDO:90062 SNOMEDCT:197270009 RGO:19820 acute liver failure RGO:19820 SNOMEDCT:123717006 RGO:19821 advanced cirrhosis RGO:19821 RGO:19822 highly trained athlete RGO:19822 RGO:19823 cavernous hemangioma of liver RGO:19823 SNOMEDCT:414795007 RGO:19827 myocardial ischemia RGO:19827 DOID:3393 HP:0001677 SNOMEDCT:53741008 RGO:19829 coronary artery disease RGO:19829 SNOMEDCT:43339004 RGO:19831 potassium depletion RGO:19831 bullae RADLEX:RID28502 SNOMEDCT:339008 RGO:19833 bulla RGO:19833 RADLEX:RID28495 SNOMEDCT:339008 SNOMEDCT:408764000 RGO:19834 bleb RGO:19834 HP:0009793 RGO:19837 presacral teratoma RGO:19837 RGO:19838 spinal lipoma RGO:19838 SNOMEDCT:59342007 RGO:19839 occupational acro-osteolysis RGO:19839 RGO:19841 localized metaphyseal injury RGO:19841 DOID:9925 HP:0004438 RGO:19843 hyperostosis frontalis interna RGO:19843 RGO:19845 chronic or healed osteomyelitis RGO:19845 RGO:19846 Garré sclerosing osteomyelitis RGO:19846 RGO:19849 Sever disease RGO:19849 ORDO:97336 RADLEX:RID5183 RGO:19850 Panner disease RGO:19850 osteonecrosis of the distal ulna RADLEX:RID29062 RGO:19854 Burns disease RGO:19854 Legg-Perthes disease Perthes disease osteochondrosis of femoral epiphysis osteonecrosis of the femoral capital epiphysis DOID:14415 ORDO:2380 RADLEX:RID5372 SNOMEDCT:111255008 RGO:19855 Legg-Calvé-Perthes disease RGO:19855 osteonecrosis of the fifth metatarsal base RADLEX:RID29070 SNOMEDCT:203395009 RGO:19856 Iselin disease RGO:19856 osteonecrosis of the greater trochanter of the femur RGO:19857 Mandl disease RGO:19857 RGO:19858 osteomyelitis with involucrum RGO:19858 RGO:19859 healing yaws RGO:19859 RGO:19861 traumatic periostitis RGO:19861 SNOMEDCT:71897006 RGO:19862 venous stasis RGO:19862 RGO:19863 lymphatic stasis RGO:19863 RGO:19864 widespread trauma RGO:19864 RGO:19865 widespread osteomyelitis RGO:19865 RGO:19866 dentino-osseous dysplasia RGO:19866 RGO:19867 unrecognized trauma RGO:19867 ICD10CM:M84.3 RADLEX:RID29139 SNOMEDCT:263253007 RGO:19868 march fracture RGO:19868 RGO:19869 multiple myeloma with pathologic fractures RGO:19869 ICD10CM:C90.0 SNOMEDCT:109989006 SNOMEDCT:55921005 RGO:19870 myelomatosis RGO:19870 RADLEX:RID3752 SNOMEDCT:261230003 SNOMEDCT:80983001 RGO:19872 bone graft RGO:19872 RGO:19873 disuse bony atrophy RGO:19873 RGO:19875 neuropathic disease RGO:19875 SNOMEDCT:373505007 SNOMEDCT:51073002 RGO:19877 phenobarbital RGO:19877 SNOMEDCT:55811003 RGO:19878 ergot RGO:19878 osteonecrosis of the head of the humerus RGO:19881 Hass disease RGO:19881 osteonecrosis of the head of the radius RADLEX:RID29060 RGO:19882 Brailsford disease RGO:19882 Mueller-Weiss syndrome osteonecrosis of the tarsal navicular DOID:11760 RADLEX:RID5371 RGO:19883 Köhler disease RGO:19883 osteonecrosis of os tibiale externum RGO:19884 Haglund disease RGO:19884 RGO:19886 osteonecrosis of the metatarsal head RGO:19886 RGO:19891 bronchial carcinoid RGO:19891 DOID:1790 HP:0100001 SNOMEDCT:109378008 SNOMEDCT:62064005 RGO:19892 malignant mesothelioma RGO:19892 RGO:19893 localized benign fibrous pleural tumor RGO:19893 COPD DOID:3083 HP:0006510 RADLEX:RID5317 SNOMEDCT:13645005 RGO:19895 chronic obstructive pulmonary disease RGO:19895 DOID:2158 RGO:19897 metastasis to lung RGO:19897 RGO:19898 osteosarcoma metastasis to lung RGO:19898 DOID:0050228 SNOMEDCT:387754006 RGO:19899 amebic dysentery RGO:19899 ferrocalcinosis DOID:0060230 RADLEX:RID5150 SNOMEDCT:110997000 RGO:19902 Fahr disease RGO:19902 SNOMEDCT:17322007 RGO:19904 parasitic disease RGO:19904 RGO:19907 birth anoxia RGO:19907 SNOMEDCT:276640009 RGO:19908 birth hypoxia RGO:19908 RGO:19909 ectopic pinealoma RGO:19909 RGO:19910 Paragonimus cyst RGO:19910 RGO:19911 Cysticercus cyst RGO:19911 DOID:5032 HP:0010799 SNOMEDCT:359619007 SNOMEDCT:47598005 RGO:19912 pinealoma RGO:19912 temporal hydrocephalus DOID:2510 ORDO:157823 RGO:19915 Klüver-Bucy syndrome RGO:19915 retinoic acid embryopathy SNOMEDCT:36871005 RGO:19920 fetal isotretinoin syndrome RGO:19920 HP:0002507 ORDO:220386 RGO:19922 semilobar holoprosencephaly RGO:19922 HP:0006870 ORDO:93924 RADLEX:RID34735 SNOMEDCT:253136007 RGO:19923 lobar holoprosencephaly RGO:19923 RGO:19925 enlarged glands of Littré RGO:19925 DOID:13558 SNOMEDCT:236682002 RGO:19926 gonococcal urethritis RGO:19926 DOID:1343 RGO:19927 non-gonococcal urethritis RGO:19927 ORDO:1911 RGO:19930 maternal cocaine abuse RGO:19930 SNOMEDCT:55912009 RGO:19933 glycogen storage disease type 5 RGO:19933 RGO:19935 congenital AIDS RGO:19935 digito-reno-cerebral syndrome RGO:19936 Eronen syndrome RGO:19936 RGO:19940 severe pyelonephritis RGO:19940 RGO:19942 interosseous ligament ossification RGO:19942 RGO:19943 familial brachydactyly A2 RGO:19943 RGO:19951 enchondromatosis with shortened ulna RGO:19951 RGO:19952 Maffucci syndrome with shortened ulna RGO:19952 fracture of radial shaft with dislocation of distal ulna RADLEX:RID29128 RGO:19953 Galeazzi fracture RGO:19953 SNOMEDCT:65966004 RGO:19955 forearm fracture RGO:19955 fracture of ulnar shaft with dislocation of radial head RADLEX:RID29140 SNOMEDCT:123973009 RGO:19956 Monteggia fracture RGO:19956 RGO:19957 bowed radius and ulna RGO:19957 RGO:19959 osteomyelitis with residual deformity RGO:19959 RGO:19960 smallpox with residual deformity RGO:19960 SNOMEDCT:418617002 RGO:19963 pelvic tilt RGO:19963 HP:0001760 RGO:19964 foot deformity RGO:19964 RGO:19965 primary vasculitis RGO:19965 DOID:2402 ICD10CM:I89.0 RADLEX:RID4748 SNOMEDCT:48087001 RGO:19970 lymphangiectasis RGO:19970 partially formed vertebra HP:0002937 RGO:19975 hemivertebra RGO:19975 SNOMEDCT:87294007 RGO:19977 supernumerary vertebra RGO:19977 false clubfoot metatarsus varus pigeon toe HP:0001840 SNOMEDCT:23568008 RGO:19980 metatarsus adductus RGO:19980 RGO:19982 tryptophan malabsorption RGO:19982 RGO:19983 active hyperthyroidism RGO:19983 RGO:19984 treated hyperthyroidism RGO:19984 SNOMEDCT:367510009 RGO:19985 ulnar drift RGO:19985 claw-hand hand contracture RGO:19998 contracted hand RGO:19998 SNOMEDCT:37097005 RGO:20002 erythroblastosis RGO:20002 SNOMEDCT:69896004 RGO:20006 rheumatoid disease RGO:20006 ORDO:99873 RADLEX:RID3848 SNOMEDCT:39795003 RGO:20008 Hand-Schüller-Christian disease RGO:20008 nonlipid histiocytosis DOID:2571 ICD10CM:C96.0 ORDO:99870 RADLEX:RID3847 SNOMEDCT:128812005 RGO:20009 Letterer-Siwe disease RGO:20009 ADEM acute disseminated encephalitis DOID:639 ORDO:83597 RADLEX:RID3415 SNOMEDCT:83942000 RGO:20012 acute disseminated encephalomyelitis RGO:20012 DOID:1602 ICD10CM:L04 SNOMEDCT:41174002 RGO:20013 acute lymphadenitis RGO:20013 RGO:20014 reactive hyperplasia of connective tissue disease RGO:20014 RGO:20015 calcification in muscles and subcutaneous tissues RGO:20015 ICD10CM:L91.0 RADLEX:RID3828 SNOMEDCT:33659008 SNOMEDCT:58405006 RGO:20016 keloid RGO:20016 RGO:20017 subungual calcification RGO:20017 RGO:20018 forearm calcification RGO:20018 RGO:20020 primary congenital lymphatic dysplasia RGO:20020 RGO:20021 atrophic hydrocephalus RGO:20021 RGO:20022 communicating nonabsorptive hydrocephalus RGO:20022 RGO:20023 noncommunicating obstructive hydrocephalus RGO:20023 HP:0002652 RADLEX:RID34679 SNOMEDCT:105986008 RGO:20026 skeletal dysplasia RGO:20026 RGO:20030 iatrogenic hemothorax RGO:20030 RADLEX:RID35815 SNOMEDCT:91602002 RGO:20031 thoracentesis RGO:20031 RGO:20032 lung biopsy RGO:20032 RGO:20033 chest tube placement RGO:20033 RADLEX:RID49618 RGO:20034 central venous catheter placement RGO:20034 RGO:20037 lacerated intercostal vessel RGO:20037 RGO:20038 chest contusion RGO:20038 RGO:20039 pleural metastasis RGO:20039 RGO:20042 uremic pleuritis RGO:20042 RGO:20044 radial head hypoplasia RGO:20044 HP:0002967 ICD10CM:M21.02 RGO:20045 cubitus valgus RGO:20045 RGO:20047 tilt of distal radius and ulna towards each other RGO:20047 SNOMEDCT:196124003 RGO:20050 alveolar capillary block RGO:20050 RGO:20051 pulmonary interstitial fibrosis RGO:20051 RGO:20052 large PDA RGO:20052 large VSD RGO:20053 large ventricular septal defect RGO:20053 RGO:20054 pulmonary AVM RGO:20054 RGO:20055 pulmonary telangiectasia RGO:20055 RGO:20056 familial brachydactyly C RGO:20056 RGO:20059 digital fibroma RGO:20059 RGO:20061 juvenile diabetes RGO:20061 RGO:20062 Bruck syndrome with congenital contractures RGO:20062 RGO:20063 third and fifth finger contractures RGO:20063 RGO:20064 acute erosive osteoarthritis RGO:20064 DOID:1586 SNOMEDCT:26424001 RGO:20067 acute rheumatic fever RGO:20067 RADLEX:RID4555 RGO:20068 synovial neoplasm RGO:20068 RGO:20071 advanced arthritis RGO:20071 ICD10CM:M36.2 SNOMEDCT:80813006 RGO:20072 hemophilic arthropathy RGO:20072 RGO:20074 postoperative arthritis RGO:20074 repair of SCFE repaired slipped capital femoral epiphysis RGO:20075 repair of slipped capital femoral epiphysis RGO:20075 RGO:20076 neuropathic arthritis RGO:20076 RGO:20077 hyperthyroidism in early childhood RGO:20077 FTT HP:0001508 SNOMEDCT:54840006 RGO:20082 failure to thrive RGO:20082 HP:0006872 RGO:20084 cerebral hypoplasia RGO:20084 Levi-Lorain syndrome DOID:9405 HP:0000839 SNOMEDCT:367460001 RGO:20085 pituitary dwarfism RGO:20085 RGO:20089 healing hypothyroidism RGO:20089 RADLEX:RID3514 SNOMEDCT:708057002 RGO:20090 sclerosing osteomyelitis RGO:20090 RGO:20091 chronic diffuse sclerosing osteomyelitis RGO:20091 RGO:20093 retained roots RGO:20093 RGO:20101 treated infantile hypothyroidism RGO:20101 SNOMEDCT:26767005 RGO:20102 bismuth poisoning RGO:20102 SNOMEDCT:81844008 RGO:20103 arsenic poisoning RGO:20103 SNOMEDCT:75529001 RGO:20104 phosphorus poisoning RGO:20104 RGO:20105 fluoride poisoning RGO:20105 SNOMEDCT:290802009 RGO:20106 lithium poisoning RGO:20106 RGO:20107 radiation injury from bone-seeking isotopes RGO:20107 RGO:20109 Sr-90 RGO:20109 RGO:20110 Y-90 RGO:20110 RGO:20111 P-32 RGO:20111 RGO:20112 healing renal osteodystrophy RGO:20112 DOID:8125 HP:0040188 RADLEX:RID5369 SNOMEDCT:19579005 RGO:20113 osteochondrosis RGO:20113 HP:0002750 RGO:20114 delayed skeletal maturation RGO:20114 RGO:20115 increased skeletal maturation RGO:20115 RGO:20120 trauma to scaphoid RGO:20120 RGO:20121 trauma to lunate RGO:20121 RGO:20126 femoral neck defect RGO:20126 DOID:4166 RADLEX:RID34765 SNOMEDCT:76272004 RGO:20129 syphilis RGO:20129 frambesia tropica polypapilloma tropicum thymosis DOID:10371 ICD10CM:A66 SNOMEDCT:70647001 RGO:20130 yaws RGO:20130 RGO:20131 boomerang tibia RGO:20131 microlithiasis of testis HP:0012215 SNOMEDCT:117261000119108 RGO:20133 testicular microlithiasis RGO:20133 RGO:20134 old hemorrhage RGO:20134 RGO:20135 cyst of testis RGO:20135 ICD10CM:N50.3 SNOMEDCT:43077002 RGO:20136 cyst of epididymis RGO:20136 SNOMEDCT:190280006 RGO:20137 phlegmon RGO:20137 DOID:10206 SNOMEDCT:93162007 RGO:20139 lipoma of spermatic cord RGO:20139 SNOMEDCT:21372000 RGO:20141 radium therapy RGO:20141 RGO:20142 arrested fetal passage RGO:20142 DOID:8494 SNOMEDCT:45757002 RGO:20143 dystocia RGO:20143 colon diverticulitis RGO:20145 colonic diverticulitis RGO:20145 DOID:0060417 RGO:20146 chromosome 3p- syndrome RGO:20146 Pitt syndrome Pitt-Rogers-Danks syndrome Wolf-Hirschhorn syndrome chromosome 4:del(4p) syndrome chromosome del (4p) syndrome chromosome del(4p) syndrome chromosome deletion Dillan 4p syndrome RGO:20147 chromosome 4p- syndrome RGO:20147 RGO:20151 familial brachydactyly A3 RGO:20151 RGO:20152 familial brachydactyly A4 RGO:20152 HP:0001371 RADLEX:RID3818 SNOMEDCT:57048009 RGO:20153 contracture RGO:20153 SNOMEDCT:367489004 RGO:20159 severe osteopetrosis RGO:20159 RGO:20161 Dandy-Walker variant RGO:20161 SNOMEDCT:399980009 RGO:20163 necrotizing angiitis RGO:20163 RGO:20164 complicated pancreatitis RGO:20164 infection of kidney SNOMEDCT:129128006 RGO:20165 kidney infection RGO:20165 RGO:20166 postoperative aortic graft infection RGO:20166 DOID:10986 RADLEX:RID3407 SNOMEDCT:2304001 RGO:20167 discitis RGO:20167 RGO:20169 postpartum infection RGO:20169 SNOMEDCT:233370007 RGO:20170 aortic aneurysm repair RGO:20170 RGO:20171 abdominal surgery RGO:20171 SNOMEDCT:425359009 RGO:20172 blunt trauma RGO:20172 RGO:20173 penetrating trauma RGO:20173 RGO:20175 fluid in iliopsoas bursa RGO:20175 RGO:20176 sarcoma of dura RGO:20176 RGO:20177 melanoma of dura RGO:20177 RADLEX:RID35511 RGO:20178 salt and pepper skull RGO:20178 RGO:20179 chronic hydrocephalus RGO:20179 RGO:20180 chronic bilateral subdural hematoma RGO:20180 RGO:20181 healed rickets RGO:20181 RGO:20182 isolated bilateral coronal synostosis RGO:20182 Lückenschädel craniolacunia RADLEX:RID35333 SNOMEDCT:29307005 RGO:20183 lacunar skull RGO:20183 RGO:20184 healed rickets with bossing RGO:20184 RGO:20186 arteriovenous fistula in prostate RGO:20186 RGO:20187 prostate biopsy RGO:20187 SNOMEDCT:74594005 RGO:20188 crossed renal ectopia RGO:20188 RGO:20189 prominent psoas muscle RGO:20189 RGO:20190 congenital ureteral stricture RGO:20190 SNOMEDCT:128060009 RGO:20191 varicosities RGO:20191 RGO:20192 sloughed calcified renal papilla RGO:20192 RGO:20194 acute arterial hypotension RGO:20194 contrast medium reaction reaction to contrast medium RGO:20197 contrast reaction RGO:20197 RGO:20198 late diabetic nephropathy RGO:20198 SNOMEDCT:311366001 RGO:20199 Kimmelstiel-Wilson syndrome RGO:20199 RGO:20200 chronic hypertension RGO:20200 SNOMEDCT:38481006 RGO:20201 hypertensive nephropathy RGO:20201 RGO:20202 chronic atrophic pyelonephritis RGO:20202 Ask-Upmark syndrome segmental renal hypoplasia RGO:20203 renal segmental hypoplasia RGO:20203 RGO:20205 bilateral renal infarction RGO:20205 RGO:20206 late cortical necrosis RGO:20206 bilateral renal vein thrombosis RGO:20207 thrombosis of renal veins RGO:20207 medullary cystic disease DOID:12712 SNOMEDCT:204957003 RGO:20209 medullary cystic kidney disease RGO:20209 RGO:20210 multiple angiomyolipomas RGO:20210 DOID:0050851 HP:0000096 SNOMEDCT:197661001 SNOMEDCT:82646005 RGO:20211 glomerulosclerosis RGO:20211 DOID:12028 SNOMEDCT:190507007 RGO:20214 primary aldosteronism RGO:20214 HP:0012408 RADLEX:RID35807 SNOMEDCT:236447005 RGO:20215 medullary nephrocalcinosis RGO:20215 RGO:20219 incomplete abortion RGO:20219 RGO:20220 recent dilatation and curettage RGO:20220 D and C dilation and curettage SNOMEDCT:11401008 RGO:20221 dilatation and curettage RGO:20221 RGO:20226 cervical atresia RGO:20226 RGO:20238 intraperitoneal fat RGO:20238 RGO:20239 extraperitoneal neoplasm RGO:20239 RGO:20240 old hemothorax RGO:20240 RGO:20241 prior empyema RGO:20241 RGO:20242 chronic hemodialysis RGO:20242 extrapleural plombage RGO:20243 oleothorax RGO:20243 RGO:20246 chronic pleural effusion RGO:20246 DOID:14305 SNOMEDCT:14527007 RGO:20247 tuberculous empyema RGO:20247 ICD10CM:K68.1 SNOMEDCT:32362007 RGO:20248 retroperitoneal abscess RGO:20248 RGO:20250 cystic renal cell carcinoma RGO:20250 facial nerve neurinoma neurinoma of facial nerve schwannoma of facial nerve RGO:20254 facial nerve schwannoma RGO:20254 RGO:20256 atresia of facial canal RGO:20256 RGO:20257 hypoplasia of facial canal RGO:20257 SNOMEDCT:57032008 RGO:20258 Pseudomonas RGO:20258 primary cholesteatoma RADLEX:RID3952 SNOMEDCT:232262007 RGO:20259 congenital cholesteatoma RGO:20259 RADLEX:RID3951 RGO:20260 acquired cholesteatoma RGO:20260 RGO:20261 temporal bone fracture RGO:20261 granular cell tumor of neurohypophysis ORDO:91353 RADLEX:RID4437 SNOMEDCT:417338002 RGO:20262 choristoma RGO:20262 HP:0200040 ICD10CM:K09.8 RADLEX:RID3907 SNOMEDCT:419670003 SNOMEDCT:419893006 RGO:20263 epidermoid cyst RGO:20263 CPA meningioma cerebellopontine angle meningioma RGO:20265 meningioma of cerebellopontine angle RGO:20265 RGO:20268 facial nerve hemangioma RGO:20268 RGO:20269 facial nerve lipoma RGO:20269 DOID:3246 HP:0006743 ORDO:99757 SNOMEDCT:14269005 SNOMEDCT:404051002 RGO:20271 embryonal rhabdomyosarcoma RGO:20271 RGO:20272 cystadenocarcinoma of endolymphatic sac RGO:20272 facial nerve sarcoma RGO:20273 sarcoma of facial nerve RGO:20273 RGO:20275 perineural spread of parotid malignancy RGO:20275 RGO:20276 perineural spread of external auditory canal malignancy RGO:20276 DOID:10755 ICD10CM:H70.2 SNOMEDCT:34997001 RGO:20280 petrositis RGO:20280 RGO:20286 aberrant internal carotid artery RGO:20286 RGO:20287 exposed internal carotid artery RGO:20287 SNOMEDCT:84499006 RGO:20288 chronic inflammation RGO:20288 RGO:20289 inflammatory debris with hemorrhage RGO:20289 RGO:20290 Wimberger ring RGO:20290 ivory epiphyses RGO:20291 dense epiphyses RGO:20291 RGO:20293 Yoruba ancestry RGO:20293 HP:0001241 RGO:20294 capitate-hamate fusion RGO:20294 HP:0009702 RGO:20295 carpal fusion RGO:20295 RGO:20296 calcaneus-cuboid fusion RGO:20296 HP:0008368 RGO:20297 tarsal fusion RGO:20297 RGO:20300 myxoid sarcoma RGO:20300 RGO:20304 spina bifida vera RGO:20304 RGO:20305 acute myelitis RGO:20305 RGO:20308 diabetic myelopathy RGO:20308 RGO:20309 trauma to spinal cord RGO:20309 DOID:10969 HP:0002301 SNOMEDCT:50582007 RGO:20310 hemiplegia RGO:20310 brain trauma RGO:20311 trauma to brain RGO:20311 SNOMEDCT:239839002 RGO:20316 idiopathic chondrocalcinosis RGO:20316 RGO:20317 chronic pyarthrosis RGO:20317 RGO:20318 degenerative osteoarthritis RGO:20318 RGO:20319 posttraumatic osteoarthritis RGO:20319 depressed hemidiaphragm flat hemidiaphragm unilateral depressed diaphragm RGO:20320 unilateral flat diaphragm RGO:20320 bilateral depressed diaphragm depressed diaphragm RGO:20321 bilateral flat diaphragm RGO:20321 RGO:20322 large unilateral intrathoracic mass RGO:20322 SNOMEDCT:16846004 RGO:20323 obstructive emphysema RGO:20323 DOID:3798 HP:0011919 RGO:20324 pleural empyema RGO:20324 RGO:20325 flat diaphragm RGO:20325 SNOMEDCT:399322006 RGO:20329 air hunger RGO:20329 RGO:20330 severe congenital heart disease RGO:20330 RGO:20331 bronchiolitis in infant RGO:20331 RGO:20332 central or bilateral foreign bodies RGO:20332 RGO:20334 intratracheal lesions RGO:20334 SNOMEDCT:425802001 RGO:20336 bilateral pleural effusion RGO:20336 RGO:20337 bilateral chylothorax RGO:20337 RGO:20338 bilateral hemothorax RGO:20338 RGO:20339 bilateral tension pneumothorax RGO:20339 RGO:20342 bilateral pulmonary thromboembolism with infarction RGO:20342 RGO:20343 bilateral rib fractures with guarding RGO:20343 RGO:20344 laryngotracheal foreign body RGO:20344 SNOMEDCT:45626005 RGO:20345 peritoneal hemorrhage RGO:20345 RGO:20347 healing hyperparathyroidism RGO:20347 SNOMEDCT:133864008 RGO:20350 lithotripsy RGO:20350 RGO:20354 reparative giant cell granuloma RGO:20354 RGO:20358 perirenal urinoma RGO:20358 HP:0030171 SNOMEDCT:197824007 RGO:20359 perirenal hematoma RGO:20359 RGO:20360 perirenal lymphocele RGO:20360 RGO:20361 acute transplant rejection RGO:20361 RGO:20363 renal transplant infection RGO:20363 RGO:20364 renal transplant ischemia RGO:20364 RGO:20365 hyperacute rejection RGO:20365 RGO:20366 hemorrhagic renal cyst RGO:20366 parapelvic cyst SNOMEDCT:431481000124104 RGO:20367 parapelvic renal cyst RGO:20367 RGO:20370 focal compensatory hypertrophy of kidney RGO:20370 RGO:20371 early tuberculosis RGO:20371 RGO:20372 focal nephrocalcinosis RGO:20372 RGO:20373 calcified renal artery aneurysm RGO:20373 RGO:20374 thrombosed renal artery aneurysm RGO:20374 RGO:20375 renal sinus duplication RGO:20375 RGO:20376 hemorrhagic pyelonephritis RGO:20376 RGO:20377 complicated renal cyst RGO:20377 RGO:20378 juxtaglomerular cell tumor RGO:20378 HP:0009726 RGO:20383 renal neoplasm RGO:20383 RGO:20384 necrotic renal cell carcinoma RGO:20384 RGO:20385 renal cyst with small mural tumor RGO:20385 RGO:20386 renal contusion RGO:20386 RGO:20387 hypertrophied coumn of Bertin RGO:20387 RGO:20388 prominent normal convolutional markings RGO:20388 RGO:20390 slow-growing intracranial tumor RGO:20390 RGO:20392 localized cerebral atrophy RGO:20392 RGO:20393 localized cerebral agenesis RGO:20393 SNOMEDCT:403996004 SNOMEDCT:52040006 RGO:20394 infantile fibrosarcoma RGO:20394 RGO:20395 chronic head-banging RGO:20395 RGO:20396 calcified cephalohematoma RGO:20396 RGO:20397 ossified subdural hematoma RGO:20397 RGO:20398 healing Langerhans cell histiocytosis RGO:20398 SNOMEDCT:23539007 RGO:20406 organizing hematoma RGO:20406 RGO:20407 neurogenic voiding dysfunction RGO:20407 RGO:20408 detrusor/external sphincter dysynergy RGO:20408 RGO:20410 acute arterial infarction RGO:20410 SNOMEDCT:205838004 SNOMEDCT:56007004 RGO:20411 congenital hemihypertrophy RGO:20411 HP:0004736 RGO:20412 crossed fused renal ectopia RGO:20412 RGO:20413 neonatal transient nephromegaly RGO:20413 RGO:20414 bilateral duplication of pelvocalyceal systems RGO:20414 RGO:20415 bilateral renal cell carcinoma RGO:20415 RGO:20416 bilateral Wilms tumor RGO:20416 RGO:20417 allergic reaction to drugs RGO:20417 SNOMEDCT:373515001 SNOMEDCT:61862008 RGO:20418 methicillin RGO:20418 SNOMEDCT:236514003 RGO:20419 toxic nephrosis RGO:20419 DOID:10966 SNOMEDCT:44785005 RGO:20420 lipoid nephrosis RGO:20420 SNOMEDCT:42927005 RGO:20421 bile nephrosis RGO:20421 RGO:20423 renal work hypertrophy RGO:20423 RGO:20424 beer-drinker kidneys RGO:20424 DOID:580 SNOMEDCT:236496000 RGO:20426 acute urate nephropathy RGO:20426 RGO:20427 subacute infective endocarditis RGO:20427 SNOMEDCT:425414000 RGO:20430 bilateral renal artery stenosis RGO:20430 RGO:20431 chronic arteritis RGO:20431 DOID:326 RADLEX:RID3376 SNOMEDCT:52674009 RGO:20432 ischemia RGO:20432 RGO:20433 postobstructive renal atrophy RGO:20433 ICD10CM:R09.01 SNOMEDCT:66466001 RGO:20435 asphyxia RGO:20435 RGO:20436 phenacetin abuse RGO:20436 RGO:20437 aspirin abuse RGO:20437 RGO:20439 renal arteritis RGO:20439 RGO:20440 renal artery thromboembolism RGO:20440 renal calculus RADLEX:RID38586 SNOMEDCT:95570007 RGO:20445 kidney stone RGO:20445 RGO:20446 stricture of infundibulum RGO:20446 RGO:20448 anomalous vessel RGO:20448 DOID:2697 SNOMEDCT:41627005 RGO:20451 renal adenoma RGO:20451 SNOMEDCT:123754002 RGO:20452 acute focal pyelonephritis RGO:20452 RGO:20453 normal renal parenchyma RGO:20453 RGO:20454 regenerated nodule RGO:20454 RADLEX:RID34632 RGO:20455 lobar dysmorphism RGO:20455 renal metastasis DOID:6995 RGO:20456 metastasis to kidney RGO:20456 RGO:20458 carcinoma of contralateral kidney RGO:20458 HP:0031625 RADLEX:RID3331 SNOMEDCT:22036004 SNOMEDCT:443089001 RGO:20459 pseudoaneurysm RGO:20459 SNOMEDCT:443416007 RGO:20460 benign adenomatous neoplasm RGO:20460 SNOMEDCT:59120003 RGO:20461 embryonal adenoma RGO:20461 DOID:2698 RADLEX:RID4542 SNOMEDCT:128760004 RGO:20462 nephrogenic adenofibroma RGO:20462 SNOMEDCT:404066004 SNOMEDCT:430750000 RGO:20464 myolipoma RGO:20464 SNOMEDCT:53880006 RGO:20465 benign hemangiopericytoma RGO:20465 reninoma RGO:20466 juxtaglomerular cell neoplasm RGO:20466 renomedullary fibroma SNOMEDCT:128761000 RGO:20468 renomedullary interstitial cell tumor RGO:20468 partial kidney resection SNOMEDCT:81516001 RGO:20473 partial nephrectomy RGO:20473 RADLEX:RID5315 SNOMEDCT:197764002 RGO:20474 reflux nephropathy RGO:20474 DOID:12577 HP:0000796 SNOMEDCT:95588004 RGO:20475 urethral obstruction RGO:20475 RGO:20477 gram-negative bacterial cystitis RGO:20477 RGO:20478 absent kidneys RGO:20478 RGO:20479 infiltrating carcinoma of bladder RGO:20479 RGO:20480 extravasated lymph RGO:20480 RGO:20481 extravasated urine RGO:20481 RADLEX:RID35423 RGO:20484 teardrop bladder RGO:20484 RADLEX:RID35423 RGO:20485 pear-shaped bladder RGO:20485 RGO:20489 gastrointestinal neoplasm RGO:20489 SNOMEDCT:446022000 RGO:20490 carcinoma of uterus RGO:20490 SNOMEDCT:254849005 RGO:20491 carcinoma of ovary RGO:20491 RADLEX:RID3918 RGO:20492 mullerian duct cyst RGO:20492 SNOMEDCT:79349002 RGO:20493 levator ani muscle RGO:20493 SNOMEDCT:68455001 RGO:20494 iliopsoas muscle RGO:20494 RADLEX:RID2606 SNOMEDCT:23937003 SNOMEDCT:304927006 RGO:20495 sacrospinous ligament RGO:20495 UJV edema edema of ureterovesical junction RGO:20497 ureterovesical junction edema RGO:20497 UVJ calculus UVJ stone RGO:20500 calculus at ureterovesical junction RGO:20500 RGO:20503 pheochromocytoma of bladder RGO:20503 RGO:20504 vaginovesical fistula RGO:20504 RGO:20505 muscular hypertrophy and trabeculation of bladder RGO:20505 RGO:20506 chronic bladder outlet obstruction RGO:20506 RADLEX:RID4824 SNOMEDCT:431771000124109 RGO:20508 Hutch diverticulum RGO:20508 RADLEX:RID1717 SNOMEDCT:265414003 RGO:20509 abdominoperineal resection RGO:20509 RADLEX:RID1764 RGO:20510 ureteral reimplantation RGO:20510 RADLEX:RID3372 SNOMEDCT:264557003 RGO:20511 ovarian vein syndrome RGO:20511 DOID:4007 SNOMEDCT:255108000 RGO:20514 carcinoma of bladder RGO:20514 RGO:20515 ureteroileal diversion RGO:20515 HP:0012409 SNOMEDCT:236446001 RGO:20518 cortical nephrocalcinosis RGO:20518 SNOMEDCT:699877004 RGO:20519 Pneumocystis carinii RGO:20519 RGO:20520 chronic hypercalcemia RGO:20520 RGO:20521 paraneoplastic hypercalcemia RGO:20521 RGO:20522 cyclamate RGO:20522 antifreeze poisoning ORDO:31826 SNOMEDCT:426692001 RGO:20523 ethylene glycol poisoning RGO:20523 SNOMEDCT:41305006 RGO:20525 secondary hyperoxaluria RGO:20525 RGO:20526 pyroxidine deficiency RGO:20526 DOID:0060236 SNOMEDCT:124147007 RGO:20527 xanthine oxidase deficiency RGO:20527 abruptio placenta DOID:9667 HP:0011419 SNOMEDCT:415105001 RGO:20529 abruptio placentae RGO:20529 RGO:20530 obstetrical bleeding complication RGO:20530 SNOMEDCT:33664007 SNOMEDCT:372709008 RGO:20532 acetazolamide RGO:20532 SNOMEDCT:714520003 SNOMEDCT:77703004 RGO:20533 amphotericin B RGO:20533 SNOMEDCT:40789008 RGO:20534 adrenocorticotrophic hormone RGO:20534 RADLEX:RID50041 SNOMEDCT:387475002 SNOMEDCT:81609008 RGO:20535 furosemide RGO:20535 SNOMEDCT:12512008 SNOMEDCT:387053007 RGO:20536 triamterene RGO:20536 DOID:1920 HP:0002149 SNOMEDCT:35885006 RGO:20538 hyperuricemia RGO:20538 RGO:20541 deToni-Fanconi syndrome RGO:20541 RGO:20543 autonephrectomy RGO:20543 RGO:20547 excessive calcium absorption RGO:20547 RGO:20548 excessive calcium intake RGO:20548 RGO:20549 widespread metastatic disease RGO:20549 RGO:20550 widespread bone destruction RGO:20550 RGO:20553 medullary fibroma RGO:20553 RGO:20556 radiodense urinary calculus RGO:20556 RGO:20557 radiolucent urinary calculus RGO:20557 RGO:20562 ammonium urate calculus RGO:20562 RGO:20563 sodium urate calculus RGO:20563 RGO:20564 magnesium urate calculus RGO:20564 RGO:20565 potassium urate calculus RGO:20565 RGO:20566 urine stasis RGO:20566 DOID:5200 SNOMEDCT:7163005 RGO:20567 urinary tract obstruction RGO:20567 RGO:20568 bone destruction RGO:20568 RGO:20569 osteolytic bone metastases RGO:20569 RGO:20573 cortical sponge kidney RGO:20573 RGO:20574 urethral valves RGO:20574 RGO:20575 lower urinary tract obstruction RGO:20575 CPDN RADLEX:RID4540 SNOMEDCT:128758001 RGO:20576 cystic partially differentiated nephroblastoma RGO:20576 RADLEX:RID1794 SNOMEDCT:90470006 RGO:20578 prostatectomy RGO:20578 RADLEX:RID1787 RGO:20579 urethroplasty RGO:20579 DOID:9339 ICD10CM:N36.5 SNOMEDCT:74944002 RGO:20580 urethral false passage RGO:20580 RADLEX:RID3900 SNOMEDCT:435301000124101 RGO:20581 communicating cyst RGO:20581 Fraley syndrome DOID:8861 RGO:20582 congenital infundibular stenosis RGO:20582 ICD10CM:N28.0 SNOMEDCT:45456005 RGO:20584 renal infarct RGO:20584 RGO:20585 inflammatory stricture RGO:20585 RGO:20586 infundibular amputation RGO:20586 squamous metaplasia of urothelium RGO:20587 urinary tract cholesteatoma RGO:20587 gas in urinary tract RGO:20589 urinary tract gas RGO:20589 RGO:20592 air from retrograde pyelogram RGO:20592 RGO:20593 percutaneous stone removal RGO:20593 RGO:20594 presacral sinus tract RGO:20594 RGO:20595 gas infection RGO:20595 RGO:20596 ureterointestinal anastomosis RGO:20596 RGO:20597 fistula to bowel RGO:20597 RGO:20598 retrograde stone removal RGO:20598 RGO:20599 sloughed papilla RGO:20599 RGO:20600 multicystic kidney with pelvoinfundibular atresia RGO:20600 RGO:20603 pyelonephritis with debris RGO:20603 RGO:20605 suppurative pyelonephritis RGO:20605 SNOMEDCT:65127006 RGO:20606 tuberculous pyelonephritis RGO:20606 RGO:20607 filling defect in calyx RGO:20607 RGO:20608 filling defect in renal pelvis RGO:20608 RGO:20609 filling defect in infundibulum RGO:20609 RGO:20610 parenchymal renal cyst RGO:20610 colon distention colonic distention distention of colon RGO:20613 distended colon RGO:20613 RGO:20615 elevated right kidney RGO:20615 RGO:20616 crossed-fused renal ectopia RGO:20616 RGO:20618 misplaced kidney RGO:20618 RGO:20619 extrarenal mass RGO:20619 RGO:20620 intracapsular extrarenal neoplasm RGO:20620 RGO:20621 lipoma of renal capsule RGO:20621 RGO:20622 thromboembolism of inferior vena cava RGO:20622 RGO:20623 thromboembolism of renal artery RGO:20623 RGO:20624 technical factors RGO:20624 RGO:20625 insufficient perinephric fat RGO:20625 RGO:20626 overlying intestinal gas RGO:20626 RADLEX:RID38611 SNOMEDCT:86273004 RGO:20627 biopsy RGO:20627 SNOMEDCT:129236007 RGO:20628 invasive procedure RGO:20628 RGO:20629 chronic end-stage renal disease RGO:20629 SNOMEDCT:177418003 RGO:20631 ruptured cyst RGO:20631 RGO:20633 renal artery branch emboli RGO:20633 RGO:20634 renal artery branch stenosis RGO:20634 RGO:20636 prominent hilar lip RGO:20636 RGO:20637 hilum profile RGO:20637 RGO:20638 prominent column of Bertin RGO:20638 RGO:20639 localized hypertrophy RGO:20639 RGO:20640 superimposed gallbladder RGO:20640 RGO:20641 superimposed duodenal bulb RGO:20641 RGO:20642 superimposed gastric fundus RGO:20642 HP:0001747 RGO:20643 superimposed accessory spleen RGO:20643 SNOMEDCT:262893009 RGO:20644 laceration of kidney RGO:20644 RGO:20645 penile squamous papilloma RGO:20645 SNOMEDCT:253907008 RGO:20646 anterior urethral valve RGO:20646 RGO:20647 urethritis cystica RGO:20647 RGO:20648 spindle cell neoplasm of retroperitoneum RGO:20648 SNOMEDCT:236513009 RGO:20649 lymphoma of kidney RGO:20649 RGO:20650 dilated perirenal lymphatics RGO:20650 RGO:20651 filariasis with chyluria RGO:20651 RADLEX:RID34425 RADLEX:RID43571 SNOMEDCT:405250000 RGO:20653 retrograde pyelography RGO:20653 RGO:20654 accidental ureteral ligation RGO:20654 RGO:20655 abdominal compression RGO:20655 SNOMEDCT:126881002 RGO:20656 neoplasm of renal pelvis RGO:20656 RGO:20658 pineal teratoma RGO:20658 HP:0007291 RGO:20659 posterior fossa cyst RGO:20659 RGO:20660 posterior fossa dermoid RGO:20660 RGO:20661 posterior fossa teratoma RGO:20661 RGO:20666 megalencephaly syndromes RGO:20666 SNOMEDCT:40720005 RGO:20671 cerebral cyst RGO:20671 RGO:20673 postural asymmetry from scoliosis RGO:20673 SNOMEDCT:64229006 RGO:20674 obstetrical trauma RGO:20674 SNOMEDCT:43349001 RGO:20675 depressed fracture RGO:20675 RGO:20676 chronic sclerotic mastoiditis RGO:20676 RGO:20677 otodystrophy RGO:20677 RGO:20678 treated Paget disease RGO:20678 DOID:9261 ICD10CM:C11 SNOMEDCT:187692001 RGO:20679 malignant neoplasm of nasopharynx RGO:20679 RGO:20685 inflammatory cholesteatoma RGO:20685 HP:0010953 RADLEX:RID4888 RGO:20687 noncommunicating hydrocephalus RGO:20687 RGO:20688 posterior fossa neoplasm RGO:20688 DOID:2124 SNOMEDCT:254935002 RGO:20689 intracranial neoplasm RGO:20689 RGO:20690 overproduction of CSF RGO:20690 RGO:20691 nonobstructive hydrocephalus RGO:20691 RGO:20692 decalcification of floor and dorsum of sella RGO:20692 RGO:20693 pointed anterior clinoids RGO:20693 RGO:20694 sellar enlargement RGO:20694 RGO:20695 thinning or loss of posterior clinoids RGO:20695 RGO:20698 partial AV communis RGO:20698 RGO:20699 complete AV communis RGO:20699 RGO:20704 circumaortic inferior vena cava RGO:20704 left IVC RGO:20705 left inferior vena cava RGO:20705 pericardial tamponade DOID:115 ICD10CM:I31.4 RADLEX:RID3283 SNOMEDCT:35304003 RGO:20707 cardiac tamponade RGO:20707 SNOMEDCT:58322009 RGO:20708 expiration RGO:20708 RGO:20709 recumbency RGO:20709 RGO:20710 traumatic azygos vein pseudoaneurysm RGO:20710 RGO:20712 traumatic aorta-pulmonary artery fistula RGO:20712 RGO:20713 postoperative aorta-pulmonary artery fistula RGO:20713 RGO:20714 ruptured aorta-pulmonary artery fistula RGO:20714 DOID:13620 HP:0001655 ORDO:99108 SNOMEDCT:204317008 RGO:20716 patent foramen ovale RGO:20716 RGO:20718 neoplasm of right atrium RGO:20718 RGO:20719 neoplasm of right ventricle RGO:20719 RGO:20720 myxoma of right ventricle RGO:20720 RGO:20721 mitral stenosis with ASD RGO:20721 RGO:20722 mitral stenosis with PDA RGO:20722 RGO:20723 mitral atresia with ASD RGO:20723 RGO:20724 mitral atresia with PDA RGO:20724 RGO:20725 aortic stenosis with PDA RGO:20725 RGO:20726 aortic stenosis with ASD RGO:20726 RGO:20727 aortic atresia with ASD RGO:20727 RGO:20728 aortic atresia with PDA RGO:20728 RGO:20729 aortic arch stenosis with ASD RGO:20729 RGO:20730 aortic arch stenosis with PDA RGO:20730 RGO:20731 aortic arch atresia with ASD RGO:20731 RGO:20732 aortic arch atresia with PDA RGO:20732 DOID:4078 HP:0010446 SNOMEDCT:49915006 RGO:20733 tricuspid stenosis RGO:20733 HP:0100645 RGO:20734 bladder hernia RGO:20734 RGO:20735 inguinal bladder hernia RGO:20735 RGO:20736 femoral bladder hernia RGO:20736 RGO:20738 aseptic cystitis RGO:20738 DOID:0050859 SNOMEDCT:87696004 RGO:20739 hemorrhagic cystitis RGO:20739 orthotopic ureterocele SNOMEDCT:204973009 RGO:20740 simple ureterocele RGO:20740 RGO:20742 segmental ureterectasis RGO:20742 RGO:20743 diffuse ureterectasis RGO:20743 ICD10CM:Q43.1 SNOMEDCT:204739008 RGO:20744 aganglionosis RGO:20744 RGO:20745 polydypsia RGO:20745 RGO:20746 congenital ureterectasis RGO:20746 RGO:20747 fusiform terminal ureterectasis RGO:20747 ORDO:617 RGO:20748 primary megaureter RGO:20748 HP:0000071 SNOMEDCT:95574003 RGO:20749 ureteral stenosis RGO:20749 irradiation postradiation postradiation change radiation effect SNOMEDCT:82107009 RGO:20753 radiation RGO:20753 RADLEX:RID4788 RGO:20754 bladder prolapse RGO:20754 SNOMEDCT:95588004 RGO:20755 obstruction of urethra RGO:20755 RGO:20757 venous collaterals RGO:20757 RGO:20758 arterial collaterals RGO:20758 SNOMEDCT:413277002 RGO:20759 postoperative stricture RGO:20759 RGO:20760 postradiation stricture RGO:20760 RGO:20761 tuberculous stricture RGO:20761 RGO:20762 iatrogenic ureteral injury RGO:20762 SNOMEDCT:44015005 RGO:20763 necrotic debris RGO:20763 RGO:20764 renal sinus mass RGO:20764 SNOMEDCT:1830000100000410 RGO:20765 complex renal cyst RGO:20765 RGO:20767 complicated simple cyst RGO:20767 RGO:20768 segmental multilocular cystic kidney RGO:20768 RGO:20769 renal vein obstruction RGO:20769 kidney fracture renal fracture RGO:20770 fractured kidney RGO:20770 RGO:20771 acute bacterial nephritis RGO:20771 SNOMEDCT:32659003 RGO:20772 congenital hypoplasia of kidney RGO:20772 RGO:20773 congenital absence of kidney RGO:20773 DOID:2972 ICD10CM:N28.0 RGO:20774 renal artery obstruction RGO:20774 HP:0001920 SNOMEDCT:302233006 RGO:20775 renal artery stenosis RGO:20775 SNOMEDCT:38481006 RGO:20776 hypertensive renal disease RGO:20776 SNOMEDCT:32278006 RGO:20779 myeloma kidney RGO:20779 AIP DOID:2800 ORDO:79126 RADLEX:RID5330 SNOMEDCT:236302005 RGO:20783 acute interstitial pneumonia RGO:20783 DOID:12522 ICD10CM:J67.1 SNOMEDCT:67242002 RGO:20790 bagassosis RGO:20790 SNOMEDCT:10446001 RGO:20793 aspergilloma RGO:20793 SNOMEDCT:182764009 RGO:20794 anticoagulant therapy RGO:20794 RGO:20795 vascular lung metastasis RGO:20795 DOID:8857 RGO:20796 lupus erythematosis RGO:20796 ICD10CM:J63.5 SNOMEDCT:51277007 RGO:20798 stannosis RGO:20798 RGO:20799 end-stage interstitial fibrosis RGO:20799 RGO:20801 compensatory renal hypertrophy RGO:20801 RGO:20803 disease of opposite kidney RGO:20803 RGO:20804 absence of opposite kidney RGO:20804 HP:0005562 SNOMEDCT:253883006 RGO:20805 multiple renal cysts RGO:20805 DOID:8736 ICD10CM:B03 SNOMEDCT:67924001 RGO:20808 smallpox RGO:20808 HP:0012317 RGO:20810 sacroiliitis RGO:20810 accessory spleen RGO:20830 splenule RGO:20830 familial Thiemann disease SNOMEDCT:55166000 RGO:20842 familial osteoarthropathy of the fingers RGO:20842 RGO:20845 granulomatous invasion of cavernous sinus RGO:20845 RGO:20853 polysplenia syndrome with complete AV canal RGO:20853 SNOMEDCT:74011000119107 RGO:20890 edema of kidney RGO:20890 RADLEX:RID5304 RGO:20891 medical renal disease RGO:20891 HP:0100581 SNOMEDCT:371011007 RGO:20893 caliectasis RGO:20893 RGO:20894 duplication with ectopic ureterocele RGO:20894 RGO:20895 cortical renal cyst RGO:20895 RGO:20896 avulsion of renal artery RGO:20896 RGO:20897 renal artery spasm RGO:20897 RGO:20898 renal compression RGO:20898 RGO:20899 extrinsic pressure on renal artery RGO:20899 RGO:20901 idiopathic renal vein thrombosis RGO:20901 RGO:20903 sarcoma of inferior vena cava RGO:20903 RGO:20904 diffuse renal inflammatory disease RGO:20904 RGO:20905 hemangioma of kidney RGO:20905 RGO:20906 acute renal artery obstruction RGO:20906 RGO:20908 necrotic Wilms tumor RGO:20908 RGO:20909 arteriovenous communication RGO:20909 DOID:4163 HP:0006747 ORDO:251877 SNOMEDCT:116381000119105 SNOMEDCT:69515008 RGO:20913 ganglioneuroblastoma RGO:20913 hereditary familial hypogonadism ICD10CM:E34.52 SNOMEDCT:58672003 RGO:20914 Reifenstein syndrome RGO:20914 RGO:20916 chronic ovarian torsion RGO:20916 DOID:2630 RADLEX:RID4152 SNOMEDCT:32140001 RGO:20918 papillary cystadenoma RGO:20918 ptosis of kidney renal ptosis RGO:20923 ptotic kidney RGO:20923 S. haematobium SNOMEDCT:3294004 RGO:20926 Schistosoma haematobium RGO:20926 SNOMEDCT:53583001 RGO:20927 Schistosoma RGO:20927 RGO:20929 urachal carcinoma RGO:20929 RGO:20931 urticarial edema RGO:20931 RGO:20933 postoperative bladder diverticulum RGO:20933 SNOMEDCT:268236002 RGO:20934 bladder neck stenosis RGO:20934 RGO:20935 air cystogram RGO:20935 RGO:20937 ureteral transposition RGO:20937 RGO:20938 ileal bladder RGO:20938 RGO:20940 postoperative hematoma RGO:20940 RGO:20941 hip replacement surgery RGO:20941 RGO:20944 bladder diversion RGO:20944 partial cystectomy RGO:20945 partial resection of bladder RGO:20945 RADLEX:RID1778 SNOMEDCT:118508005 SNOMEDCT:264363008 RGO:20946 ileal conduit RGO:20946 ICD10CM:N39.498 SNOMEDCT:78459008 RGO:20948 total incontinence RGO:20948 SNOMEDCT:48340000 RGO:20950 incontinence RGO:20950 RGO:20951 inferior vena cava obstruction with venous collaterals RGO:20951 Cytoxan SNOMEDCT:387420009 SNOMEDCT:74470007 RGO:20952 cyclophosphamide RGO:20952 RGO:20954 adrenal metastasis RGO:20954 RGO:20955 multiple primary carcinomas RGO:20955 RGO:20956 cystic adrenal neoplasm RGO:20956 RGO:20957 cystic pheochromocytoma RGO:20957 RGO:20958 necrotic adrenal neoplasm RGO:20958 RGO:20960 functioning adrenal adenoma RGO:20960 RGO:20961 nonfunctioning adrenal adenoma RGO:20961 RGO:20962 cystic degeneration in benign prostatic hypertrophy RGO:20962 RGO:20964 TURP RGO:20964 ICD10CM:N41.0 SNOMEDCT:79411002 RGO:20965 acute prostatitis RGO:20965 DOID:11535 ICD10CM:N42.3 SNOMEDCT:445068007 RGO:20966 dysplasia of prostate RGO:20966 DOID:2301 SNOMEDCT:29524003 RGO:20967 atrophy of prostate RGO:20967 RGO:20968 BCG prostatitis RGO:20968 RGO:20969 clustered prostate retention cysts RGO:20969 RGO:20970 prominent ejaculatory ducts RGO:20970 BCG RGO:20971 bacillus Calmette-Guerin RGO:20971 SNOMEDCT:236768005 RGO:20973 chronic epididymitis RGO:20973 RGO:20974 chronic seminal vesiculitis RGO:20974 RGO:20975 dilated lymphatics RGO:20975 SNOMEDCT:24076008 RGO:20977 Armillifer RGO:20977 SNOMEDCT:3824001 RGO:20978 guinea worm RGO:20978 SNOMEDCT:33359002 RGO:20979 degenerative change RGO:20979 SNOMEDCT:410021007 RGO:20980 urethral catheterization RGO:20980 utricle utriculus masculinus RADLEX:RID38896 SNOMEDCT:84140001 RGO:20981 prostatic utricle RGO:20981 SNOMEDCT:285312008 RGO:20982 carcinoma of sigmoid colon RGO:20982 SNOMEDCT:254893005 RGO:20983 carcinoma of vagina RGO:20983 RGO:20984 carcinoma of uterus RGO:20984 RGO:20985 carcinoma of bladder RGO:20985 RGO:20986 strictures RGO:20986 RGO:20987 osteocartilaginous metaplasia after ureterotomy RGO:20987 RGO:20988 sacral lesion RGO:20988 RGO:20989 lesion of bony pelvis RGO:20989 RGO:20991 surgical ligature RGO:20991 RGO:20992 postoperative edema RGO:20992 SNOMEDCT:126882009 RGO:20993 neoplasm of ureter RGO:20993 congenital UPJ obstruction RGO:20994 congenital ureteropelvic junction obstruction RGO:20994 RGO:20999 intraspinal cyst RGO:20999 RGO:21000 widening of spinal cord RGO:21000 ORDO:139417 SNOMEDCT:47000000 RGO:21001 acute transverse myelitis RGO:21001 SNOMEDCT:25044007 RGO:21003 Devic syndrome RGO:21003 RADLEX:RID3608 RGO:21006 seronegative spondyloarthropathy RGO:21006 RGO:21010 rheumatoid monoarthritis RGO:21010 RGO:21011 sympathetic joint effusion RGO:21011 SNOMEDCT:462172006 RGO:21012 fetal heart failure RGO:21012 RGO:21013 atrioventricular shunt RGO:21013 RGO:21015 myocardial disorder RGO:21015 RGO:21016 placental tumor RGO:21016 RGO:21017 interruption of aorta RGO:21017 RGO:21018 short limb dwarf syndrome RGO:21018 Cori disease Cori-Forbes disease Forbes disease Forbes-Cori disease SNOMEDCT:66937008 RGO:21027 glycogen storage disease type 3 RGO:21027 RGO:21028 sialocyst RGO:21028 large tongue HP:0000158 ICD10CM:Q38.2 SNOMEDCT:25273001 RGO:21029 macroglossia RGO:21029 DOID:10016 SNOMEDCT:61530001 RGO:21030 mucosal neuroma syndrome RGO:21030 ICD10CM:M31.0 RADLEX:RID3688 SNOMEDCT:60555002 RGO:21031 hypersensitivity angiitis RGO:21031 RGO:21034 secondary degenerative arthritis RGO:21034 RGO:21035 primary degenerative arthritis RGO:21035 RGO:21037 early septic arthritis RGO:21037 DOID:801 HP:0005261 ICD10CM:M25.0 RADLEX:RID4703 SNOMEDCT:81808003 RGO:21038 hemarthrosis RGO:21038 transient synovitis ICD10CM:M67.3 SNOMEDCT:202924004 RGO:21040 toxic synovitis RGO:21040 RGO:21042 serous joint effusion RGO:21042 RGO:21049 cryoagglutination RGO:21049 RGO:21050 polyvinylchloride poisoning RGO:21050 HP:0001647 ICD10CM:Q23.1 SNOMEDCT:72352009 RGO:21051 bicuspid aortic valve RGO:21051 RGO:21053 arteritis necrotizing vasculitis RGO:21053 RGO:21054 metamphetamine abuse RGO:21054 RGO:21056 atrial myxoma embolization RGO:21056 RGO:21060 pulmonary artery coarctation RGO:21060 ICD10CM:E88.01 ORDO:60 SNOMEDCT:30188007 RGO:21063 alpha-1-antitrypsin deficiency RGO:21063 ORDO:228116 RGO:21064 Hughes-Stovin syndrome RGO:21064 DOID:1314 SNOMEDCT:288517002 RGO:21066 wasting disease RGO:21066 HP:0004326 ICD10CM:R64 SNOMEDCT:238108007 RGO:21067 cachexia RGO:21067 RGO:21071 left ventricular outflow obstruction RGO:21071 SNOMEDCT:29899005 RGO:21072 coronary embolism RGO:21072 DOID:11847 SNOMEDCT:398274000 RGO:21073 coronary thrombosis RGO:21073 RGO:21074 degeneration of xenograft RGO:21074 RGO:21075 degeneration of homograft RGO:21075 RGO:21076 hypertrophy from bladder outlet obstruction RGO:21076 RGO:21080 acrocephalosyndactyly Pfeiffer type RGO:21080 RGO:21082 acute hemorrhagic pyelonephritis RGO:21082 RGO:21083 healing infarction RGO:21083 RADLEX:RID49839 SNOMEDCT:286628000 RGO:21088 nephrostomy tube RGO:21088 RGO:21089 ureteral stent RGO:21089 renal moniliasis SNOMEDCT:370368007 RGO:21090 renal candidiasis RGO:21090 RGO:21091 metastasis to adrenal RGO:21091 scrotal fibroma RGO:21093 fibrous pseudotumor RGO:21093 RGO:21095 post-orchitis fibrosis RGO:21095 SNOMEDCT:399340005 RGO:21097 hereditary glomerulonephritis RGO:21097 RGO:21098 bacterial glomerulonephritis RGO:21098 SNOMEDCT:106911000119102 RGO:21099 idiopathic glomerulonephritis RGO:21099 HP:0011560 ORDO:1205 SNOMEDCT:23063005 RGO:21100 mitral atresia RGO:21100 RGO:21101 severe mitral stenosis RGO:21101 RGO:21103 Taussig-Bing anomaly RGO:21103 RGO:21104 interventricular septum rupture RGO:21104 degenerative abdominal aortic aneurysm with periarterial fibrosis SNOMEDCT:261850007 RGO:21107 inflammatory aneurysm RGO:21107 RGO:21110 pulmonary artery pseudoaneurysm RGO:21110 RGO:21112 large left-to-right shunt RGO:21112 SNOMEDCT:87161003 RGO:21113 medial degeneration RGO:21113 circumaortic renal collar RGO:21117 circumaortic left renal veins RGO:21117 RGO:21124 prenatal foramen ovale closure RGO:21124 RGO:21125 treated hypothyroidism RGO:21125 RGO:21126 severe acute arterial obstruction RGO:21126 RGO:21129 renal transplant hypertrophy RGO:21129 RGO:21132 allergic angiitis RGO:21132 SNOMEDCT:11791001 RGO:21133 necrotizing vasculitis RGO:21133 RGO:21135 intravenous contrast media RGO:21135 RGO:21137 total renal infarction RGO:21137 RGO:21138 lobar renal infarction RGO:21138 RGO:21139 postinflammatory atrophy following acute bacterial nephritis RGO:21139 RADLEX:RID34618 SNOMEDCT:378007 RGO:21140 Morquio disease RGO:21140 RGO:21142 carpal and tarsal osteolysis RGO:21142 fused vertebra HP:0002948 RGO:21143 fused vertebrae RGO:21143 RGO:21144 isolated spinal anomaly RGO:21144 block vertebra block vertebrae RGO:21145 congenital fused vertebrae RGO:21145 RGO:21146 acquired fused vertebrae RGO:21146 RGO:21149 spinal infection RGO:21149 RGO:21150 healed juvenile discitis RGO:21150 RGO:21152 non-weight bearing RGO:21152 RGO:21156 micrognathic dwarfism RGO:21156 RGO:21157 paraspinal abscess RGO:21157 DOID:6590 RADLEX:RID5116 SNOMEDCT:84172003 RGO:21158 spondylitis RGO:21158 RGO:21159 neoplasm of spine RGO:21159 ICD10CM:N34.0 SNOMEDCT:55069005 RGO:21163 periurethral abscess RGO:21163 RGO:21164 displacement of kidney RGO:21164 RGO:21165 colonic neoplasm RGO:21165 RGO:21166 extraperitoneal effusion RGO:21166 DOID:409 HP:0001392 RADLEX:RID34712 SNOMEDCT:235856003 RGO:21167 liver disease RGO:21167 RGO:21169 hematogenous infection of kidney RGO:21169 RGO:21170 renal corticomedullary abscess RGO:21170 focal bacterial pyelonephritis focal pyelonephritis lobar nephronia nephronia RGO:21171 acute focal bacterial nephritis RGO:21171 RGO:21172 acute multifocal bacterial nephritis RGO:21172 osteonecrosis of the iliac crest RADLEX:RID29061 RGO:21174 Buchman disease RGO:21174 RGO:21175 chronic infection of bladder RGO:21175 RGO:21176 alkaline-encrusted cystitis RGO:21176 RGO:21177 mitomycin C instillation RGO:21177 RGO:21178 rectal colloid carcinoma RGO:21178 SNOMEDCT:54493002 RGO:21179 intramural hematoma RGO:21179 RGO:21181 Foley catheter RGO:21181 RGO:21182 mixed mesodermal neoplasm RGO:21182 RGO:21183 mural edema RGO:21183 RGO:21184 impacted ureteral calculus RGO:21184 RGO:21185 mural hemorrhage RGO:21185 SNOMEDCT:31069005 RGO:21186 fibrous polyp RGO:21186 RGO:21187 ureteral anastomosis RGO:21187 RGO:21189 perforated calculus RGO:21189 SNOMEDCT:129249002 RGO:21190 needle biopsy RGO:21190 RGO:21191 fibromuscular disease RGO:21191 RGO:21193 spontaneous rupture of kidney RGO:21193 SNOMEDCT:45456005 RGO:21194 renal infarction RGO:21194 SNOMEDCT:2247000100000410 RGO:21195 ruptured renal cyst RGO:21195 RGO:21199 large psoas muscle RGO:21199 RGO:21200 spinal lesion RGO:21200 RGO:21202 retroperitoneal lymph node enlargement RGO:21202 HP:0000081 RGO:21203 duplicated renal collecting system RGO:21203 RGO:21204 colloid colon carcinoma RGO:21204 RGO:21205 calcified sloughed renal papilla RGO:21205 umbilical cord hydrops RGO:21206 umbilical cord edema RGO:21206 RGO:21208 pseudogestational sac RGO:21208 RGO:21209 gestational sac RGO:21209 RGO:21210 congenital rib hypoplasia RGO:21210 RGO:21214 necrotic renal neoplasm RGO:21214 RGO:21215 cystic renal neoplasm RGO:21215 RGO:21218 infection with necrosis RGO:21218 RGO:21221 maternal cardiovascular disease RGO:21221 HP:0008071 SNOMEDCT:288250001 RGO:21222 maternal hypertension RGO:21222 RGO:21223 maternal renal disease RGO:21223 RGO:21224 toxemia RGO:21224 HP:0001790 RGO:21225 nonimmune hydrops RGO:21225 RGO:21227 maternal anemia RGO:21227 DOID:3590 ICD10CM:O01 ORDO:99927 RADLEX:RID4331 SNOMEDCT:417044008 SNOMEDCT:48430004 RGO:21232 hydatidiform mole RGO:21232 SNOMEDCT:71837009 RGO:21233 cytotoxic drug RGO:21233 SNOMEDCT:38314008 SNOMEDCT:387208003 RGO:21234 isotretinoin RGO:21234 SNOMEDCT:80056000 RGO:21235 aneuploidy RGO:21235 RGO:21236 maternal renal failure RGO:21236 RGO:21237 structural anomaly RGO:21237 RGO:21238 placental vascular insufficiency RGO:21238 DOID:7420 HP:0011416 ICD10CM:O43.81 SNOMEDCT:268585006 RGO:21239 placental infarction RGO:21239 RGO:21240 fetal chromosomal abnormality RGO:21240 RGO:21244 maternal malnutrition RGO:21244 SNOMEDCT:428561000124100 RGO:21245 maternal substance abuse RGO:21245 ICD10CM:Z72.0 SNOMEDCT:110483000 RGO:21246 tobacco use RGO:21246 RGO:21247 maternal age greater than 35 years RGO:21247 RGO:21248 maternal age less than 17 years RGO:21248 SNOMEDCT:203985009 RGO:21249 cervical meningomyelocele RGO:21249 RGO:21250 nonfused amnion RGO:21250 RGO:21251 nuchal thickening RGO:21251 SNOMEDCT:85974009 RGO:21252 intracranial mass RGO:21252 DOID:1319 HP:0030692 RGO:21253 brain neoplasm RGO:21253 RGO:21254 fetal abdominal mass RGO:21254 SNOMEDCT:126851005 RGO:21255 hepatic tumor RGO:21255 RGO:21256 maternal pelvic mass RGO:21256 SNOMEDCT:169957005 RGO:21257 placental abnormality RGO:21257 HP:0001561 SNOMEDCT:86203003 RGO:21258 hydramnios RGO:21258 RGO:21260 normal bowel herniation RGO:21260 RADLEX:RID43412 SNOMEDCT:440299000 RGO:21261 chest mass RGO:21261 HP:0031500 SNOMEDCT:271860004 RGO:21262 abdominal mass RGO:21262 RGO:21263 fetal arteriovenous fistula RGO:21263 RGO:21265 non-teratomatous germ cell tumor RGO:21265 SNOMEDCT:176747002 RGO:21266 culdocentesis RGO:21266 RGO:21269 functional cyst RGO:21269 HP:0012886 SNOMEDCT:119420007 RGO:21270 hemorrhagic ovarian cyst RGO:21270 RGO:21271 postoperative abscess RGO:21271 DOID:3269 RGO:21272 ovarian cystadenoma RGO:21272 RGO:21273 degenerated uterine fibroid RGO:21273 RGO:21274 pedunculated uterine fibroid RGO:21274 RGO:21275 torsed uterine fibroid RGO:21275 DOID:5563 RADLEX:RID4323 SNOMEDCT:19467007 RGO:21276 immature teratoma RGO:21276 DOID:4001 HP:0025318 RGO:21277 ovarian carcinoma RGO:21277 dermoid cyst of ovary DOID:5117 HP:0025274 RGO:21278 ovarian dermoid cyst RGO:21278 DOID:2871 HP:0012114 SNOMEDCT:254878006 RGO:21281 endometrial carcinoma RGO:21281 adenomyosis adenomyosis of uterus ectopic hemorrhagic endometrial rests endometriosis of uterus DOID:288 RGO:21282 uterine adenomyosis RGO:21282 acute PID SNOMEDCT:237037006 RGO:21286 acute pelvic inflammatory disease RGO:21286 RGO:21288 intrauterine hemorrhage RGO:21288 SNOMEDCT:64779008 RGO:21289 coagulation disorder RGO:21289 RGO:21292 acute contrast nephropathy RGO:21292 SNOMEDCT:53248001 RGO:21294 ureteral catheterization RGO:21294 RGO:21295 severe acute pyelonephritis RGO:21295 RGO:21296 acute renal arterial insufficiency RGO:21296 RGO:21298 sulfonamide therapy RGO:21298 DOID:582 HP:0003641 ICD10CM:R82.3 SNOMEDCT:68600005 RGO:21299 hemoglobinuria RGO:21299 SNOMEDCT:236495001 RGO:21300 urate nephropathy RGO:21300 RGO:21302 renal laceration RGO:21302 SNOMEDCT:197813005 RGO:21303 intrarenal hematoma RGO:21303 RGO:21304 arterial branch occlusion RGO:21304 RGO:21306 congenital infundibular obstruction RGO:21306 DOID:2974 SNOMEDCT:204962002 RGO:21307 multicystic kidney RGO:21307 RGO:21309 empty stomach RGO:21309 RGO:21311 intestinal obstruction with perforation RGO:21311 SNOMEDCT:94659001 RGO:21314 metastasis to ureter RGO:21314 RGO:21315 direct invasion by extrinsic malignancy RGO:21315 RGO:21316 ureteral metastasis RGO:21316 RGO:21318 carcinoma of intestinal tract RGO:21318 RGO:21319 varices of gonad RGO:21319 RGO:21320 varices of ureter RGO:21320 RGO:21321 varices of broad ligament RGO:21321 SNOMEDCT:236709004 RGO:21322 calculus in calyceal diverticulum RGO:21322 RGO:21323 milk of calcium in calyceal diverticulum RGO:21323 SNOMEDCT:81363003 RGO:21324 malignant arteriolar nephrosclerosis RGO:21324 SNOMEDCT:233854003 RGO:21325 atrial myxoma RGO:21325 RGO:21326 hemorrhagic renal infarction RGO:21326 RGO:21328 cyst containing debris RGO:21328 RGO:21329 hemorhagic cyst RGO:21329 RGO:21330 focal infarction RGO:21330 DOID:8515 HP:0001648 RADLEX:RID3282 SNOMEDCT:83291003 RGO:21331 cor pulmonale RGO:21331 RGO:21332 chronic left heart failure RGO:21332 HP:0001667 SNOMEDCT:89792004 RGO:21333 right ventricular hypertrophy RGO:21333 RGO:21334 congenital atriomegaly RGO:21334 SNOMEDCT:36665001 RGO:21335 atrial aneurysm RGO:21335 RGO:21336 ruptured sinus of Valsalva aneurysm RGO:21336 DOID:9477 RADLEX:RID4834 RGO:21340 pulmonary embolus RGO:21340 HP:0030957 SNOMEDCT:253577002 RGO:21341 ventricular septal aneurysm RGO:21341 RGO:21342 ventricular septal diverticulum RGO:21342 RGO:21343 idiopathic myocardial hypertrophy RGO:21343 SNOMEDCT:118507000 RGO:21346 thymus gland RGO:21346 DOID:3275 HP:0100522 ORDO:99867 RADLEX:RID4278 SNOMEDCT:128856005 SNOMEDCT:444231005 RGO:21347 thymoma RGO:21347 ICD10CM:J92 RADLEX:RID43269 SNOMEDCT:233658003 RGO:21348 pleural plaque RGO:21348 SNOMEDCT:126734005 RGO:21349 neoplasm of pericardium RGO:21349 ORDO:99102 RGO:21350 left atrial appendage enlargement RGO:21350 RGO:21352 pericardial adhesion RGO:21352 RGO:21353 pulmonary artery conduit RGO:21353 RGO:21358 left-sided ascending aorta RGO:21358 RGO:21359 inverted rudimentary right ventricle RGO:21359 DOID:0050891 HP:0008256 RGO:21360 adrenocortical adenoma RGO:21360 Conn syndrome DOID:12028 DOID:446 HP:0011736 ICD10CM:E26.0 SNOMEDCT:190507007 RGO:21361 primary hyperaldosteronism RGO:21361 DOID:10825 SNOMEDCT:59621000 RGO:21362 essential hypertension RGO:21362 ORDO:96253 SNOMEDCT:190502001 RGO:21363 Cushing disease RGO:21363 SNOMEDCT:126880001 RGO:21364 renal tumor RGO:21364 DOID:14766 HP:0000104 RADLEX:RID34645 SNOMEDCT:204942005 RGO:21365 renal agenesis RGO:21365 HP:0000089 ORDO:93101 SNOMEDCT:32659003 RGO:21366 renal hypoplasia RGO:21366 RGO:21367 pharmacologic hypertension RGO:21367 RGO:21368 estrogen-containing oral contraceptives RGO:21368 RGO:21369 psychogenic hypertension RGO:21369 RGO:21370 neurogenic hypertension RGO:21370 RGO:21371 compression of coronary artery RGO:21371 RGO:21372 os centrale RGO:21372 RGO:21374 extra distal carpals RGO:21374 RGO:21375 os triangulare RGO:21375 RGO:21376 irregular carpal margins RGO:21376 HP:0002656 SNOMEDCT:254080004 RGO:21377 epiphyseal dysplasia RGO:21377 RGO:21378 abnormally shaped scaphoid RGO:21378 RGO:21380 absent or hypoplastic scaphoid RGO:21380 RGO:21381 scaphoid fused to other carpals RGO:21381 RGO:21382 abnormally shaped capitate RGO:21382 RGO:21383 absent or hypoplastic capitate RGO:21383 HP:0001234 RADLEX:RID35276 RGO:21384 hitchhiker thumb RGO:21384 SNOMEDCT:1156003 RGO:21385 cavitary prostatitis RGO:21385 RGO:21386 hormonal therapy RGO:21386 RGO:21387 testicular cyst RGO:21387 RGO:21388 vas deferens cyst RGO:21388 ICD10CM:N49.3 RADLEX:RID3448 SNOMEDCT:398318005 RGO:21390 Fournier gangrene RGO:21390 appendix testis RGO:21391 hydatid of Morgagni RGO:21391 ORDO:10 SNOMEDCT:403760006 RGO:21393 XXYY syndrome RGO:21393 49,XXXYY syndrome ORDO:261534 RGO:21394 XXXYY syndrome RGO:21394 RGO:21396 cystic testicular neoplasm RGO:21396 RGO:21397 necrotic testicular neoplasm RGO:21397 RGO:21398 simple testicular cyst RGO:21398 dilatation of rete testis RGO:21399 intratesticular tubular ectasia RGO:21399 DOID:1037 SNOMEDCT:128822004 RGO:21401 lymphoblastic leukemia RGO:21401 DOID:4136 SNOMEDCT:28351005 RGO:21403 myxosarcoma RGO:21403 DOID:2668 RADLEX:RID4533 SNOMEDCT:44524009 RGO:21404 mesenchymoma RGO:21404 RGO:21406 lymphoma metastasis RGO:21406 RGO:21407 leukemia metastasis RGO:21407 neoplasm of heart HP:0100544 RGO:21409 cardiac neoplasm RGO:21409 DOID:820 HP:0012819 RADLEX:RID3503 SNOMEDCT:50920009 RGO:21412 myocarditis RGO:21412 RGO:21413 high output heart disease RGO:21413 RGO:21414 renovascular disease RGO:21414 RGO:21415 dextroversion with situs solitus RGO:21415 RGO:21418 burned-out germ cell tumor RGO:21418 DOID:3089 SNOMEDCT:50390006 RGO:21419 granulomatous orchitis RGO:21419 RGO:21421 testicular tumor after treatnment RGO:21421 ICD10CM:Q51.3 RADLEX:RID39210 SNOMEDCT:31401003 RGO:21422 bicornate uterus RGO:21422 HP:0003762 ORDO:180086 RADLEX:RID39255 SNOMEDCT:15545001 RGO:21423 uterus didelphys RGO:21423 SNOMEDCT:13867009 RGO:21424 preductal coarctation of aorta RGO:21424 SNOMEDCT:72242008 RGO:21425 postductal coarctation of aorta RGO:21425 HP:0030812 SNOMEDCT:249395001 RGO:21426 enlarged tonsils RGO:21426 SNOMEDCT:73430006 RGO:21427 sleep apnea syndrome RGO:21427 DOID:0060311 RGO:21428 enlarged adenoids RGO:21428 DOID:3241 SNOMEDCT:416916004 RGO:21429 lipid pneumonia RGO:21429 SNOMEDCT:38877003 RGO:21430 rheumatoid aortitis RGO:21430 DOID:0060000 HP:0006689 SNOMEDCT:233850007 RGO:21431 infective endocarditis RGO:21431 SNOMEDCT:9250002 RGO:21438 celiac axis compression syndrome RGO:21438 DOID:8675 RADLEX:RID3840 SNOMEDCT:188498009 RGO:21440 lymphosarcoma RGO:21440 RGO:21441 perforation of vessel RGO:21441 SNOMEDCT:22625005 RGO:21442 hemomediastinum RGO:21442 RGO:21443 local infection RGO:21443 RADLEX:RID4386 SNOMEDCT:19071004 RGO:21448 leiomyoblastoma RGO:21448 RGO:21453 renal medullary fibroma RGO:21453 RGO:21454 renal medullary tumor RGO:21454 DOID:0050922 HP:0002672 RGO:21455 gastrointestinal carcinoma RGO:21455 RADLEX:RID39270 SNOMEDCT:44598004 RGO:21457 fibromyoma RGO:21457 RADLEX:RID4347 SNOMEDCT:2710003 RGO:21458 fibrolipoma RGO:21458 DOID:4235 SNOMEDCT:9801004 RGO:21460 spindle cell sarcoma RGO:21460 DOID:4464 ORDO:319319 RGO:21463 renal medullary carcinoma RGO:21463 RGO:21465 calcific aortic stenosis RGO:21465 HP:0001674 SNOMEDCT:341079007 SNOMEDCT:77469004 RGO:21468 atrioventricular canal RGO:21468 RGO:21470 double outlet right ventricle without PS RGO:21470 RGO:21473 elevation of hemidiaphragm RGO:21473 DOID:3770 HP:0002206 SNOMEDCT:51615001 RGO:21475 pulmonary fibrosis RGO:21475 RGO:21476 idiopathic primary pulmonary hypertension RGO:21476 RGO:21477 pulmonary arteriolar sclerosis RGO:21477 SNOMEDCT:86318000 RGO:21478 decreased cardiac output RGO:21478 RGO:21479 idiopathic aortomegaly RGO:21479 SNOMEDCT:8725005 RGO:21481 prostatic abscess RGO:21481 SNOMEDCT:52490000 RGO:21482 theca cell tumor RGO:21482 RGO:21484 follicular ovarian cyst RGO:21484 RGO:21485 mucinous ovarian cystadenocarcinoma RGO:21485 DOID:3267 RGO:21486 mucinous ovarian cystadenoma RGO:21486 HP:0002891 ORDO:213625 RGO:21487 uterine leiomyosarcoma RGO:21487 RGO:21488 small bowel tuberculosis RGO:21488 SNOMEDCT:78167007 RGO:21490 Cysticercus RGO:21490 RADLEX:RID5640 SNOMEDCT:83418008 RGO:21491 fetus RGO:21491 RGO:21492 placental calcification RGO:21492 RGO:21493 calcified omental fat RGO:21493 RGO:21494 calcified epiploic appendage RGO:21494 RGO:21496 diffuse emphysema RGO:21496 vanishing lung disease RADLEX:RID28503 SNOMEDCT:195957006 RGO:21497 bullous emphysema RGO:21497 RGO:21499 mechanical obstruction of tricuspid valve RGO:21499 myxoma of right atrium RGO:21500 right atrial myxoma RGO:21500 RGO:21501 renal cell carcinoma extending into right atrium RGO:21501 RGO:21502 compression of pulmonary artery RGO:21502 RGO:21503 marked tricuspid insufficiency RGO:21503 HP:0001708 SNOMEDCT:367363000 RGO:21504 right ventricular failure RGO:21504 RGO:21505 severe pulmonary valvular stenosis RGO:21505 RGO:21506 diffuse pulmonary embolism RGO:21506 RGO:21507 trophoblastic embolic metastases RGO:21507 RGO:21508 congenital aneurysm of coronary artery RGO:21508 RGO:21509 iatrogenic injury RGO:21509 HP:0006702 ICD10CM:I25.42 SNOMEDCT:233998004 RGO:21510 coronary artery dissection RGO:21510 RGO:21513 transient viral synovitis RGO:21513 RGO:21516 pyometrocolpos RGO:21516 false pregnancy RGO:21517 pseudocyesis RGO:21517 fibroid uterus fibroids fibroids of uterus uterine leiomyomas uterine leiomyomata SNOMEDCT:44598004 SNOMEDCT:95315005 RGO:21519 uterine fibroids RGO:21519 RGO:21525 endometrial calcification RGO:21525 RGO:21526 endometrial infection RGO:21526 RGO:21527 gas from recent instrumentation RGO:21527 ICD10CM:A18.17 SNOMEDCT:35585004 RGO:21529 tuberculous endometritis RGO:21529 degenerating fibroid degenerating leiomyoma RGO:21530 degenerating uterine fibroid RGO:21530 RGO:21531 invasive ovarian carcinoma RGO:21531 RGO:21532 early multiple gestation RGO:21532 RGO:21533 normal menses RGO:21533 RGO:21535 seminal vesicle calcification RGO:21535 RGO:21536 fallopian tube calcification RGO:21536 RGO:21537 idiopathic calcification RGO:21537 RGO:21539 infected uterine fibroid RGO:21539 HP:0100590 ICD10CM:K60.4 SNOMEDCT:80736008 RGO:21540 rectal fistula RGO:21540 RGO:21541 rectal laceration RGO:21541 SNOMEDCT:7415003 RGO:21542 ovarian abscess RGO:21542 RGO:21543 cervical carcinoma with intestinal fistula RGO:21543 RGO:21544 endometrial carcinoma with intestinal fistula RGO:21544 RGO:21545 pneumatosis cystoides of sigmoid colon RGO:21545 RGO:21551 fluid-filled bowel loop RGO:21551 RGO:21552 uterine carcinoma RGO:21552 HP:0012226 SNOMEDCT:716077006 RGO:21553 ovarian teratoma RGO:21553 RGO:21558 intramural injection of contrast medium RGO:21558 RGO:21559 cutix laxa RGO:21559 RGO:21560 catheterization injury RGO:21560 SNOMEDCT:473360003 RGO:21561 left atrial thrombus RGO:21561 RGO:21562 left atrial ball-valve thrombus RGO:21562 RGO:21563 airway obstruction RGO:21563 RGO:21564 laryngeal airway obstruction RGO:21564 left ventricular hypertrophy encroaching on right ventricle SNOMEDCT:13839000 RGO:21565 Bernheim syndrome RGO:21565 SNOMEDCT:373095005 RGO:21569 coronary artery fistula to right atrium RGO:21569 SNOMEDCT:373096006 RGO:21570 coronary artery fistula to right ventricle RGO:21570 RGO:21572 truncus arteriosus with single pulmonary artery RGO:21572 RADLEX:RID28537 SNOMEDCT:76171001 RGO:21573 air trapping RGO:21573 RGO:21574 hypogenetic lung RGO:21574 HP:0004935 SNOMEDCT:204443008 RGO:21575 pulmonary artery atresia RGO:21575 DOID:5200 RGO:21578 urinary obstruction RGO:21578 RGO:21579 extrinsic compression of kidney RGO:21579 HP:0000103 ICD10CM:R35 SNOMEDCT:28442001 RGO:21580 polyuria RGO:21580 RGO:21581 diabetes mellitus with renal disease RGO:21581 RGO:21582 renal gas RGO:21582 RGO:21583 calcified renal cyst RGO:21583 RGO:21586 renal artery calcification RGO:21586 RGO:21587 calcified sloughed papilla RGO:21587 RGO:21588 phrenic nerve injury RGO:21588 RGO:21591 infectious myocarditis RGO:21591 RGO:21592 coxsackie virus RGO:21592 RGO:21596 collateral paraureteral artery RGO:21596 SNOMEDCT:312496009 RGO:21598 iliac artery stenosis RGO:21598 SNOMEDCT:314187004 RGO:21599 iliac artery occlusion RGO:21599 RGO:21600 collateral paraureteral vein RGO:21600 RGO:21602 gonadal vein obstruction RGO:21602 RGO:21603 azygos vein obstruction RGO:21603 RADLEX:RID1567 SNOMEDCT:34564005 RGO:21605 Waterston shunt RGO:21605 SNOMEDCT:86642005 RGO:21606 Potts shunt RGO:21606 RGO:21607 transposition of great vessels with VSD and pulmonary stenosis RGO:21607 RGO:21608 transposition of great vessels with VSD and pulmonary atresia RGO:21608 RGO:21609 tricuspid atresia with pulmonary atresia RGO:21609 RGO:21610 tricuspid atresia with pulmonary stenosis RGO:21610 RGO:21611 tricuspid stenosis with pulmonary atresia RGO:21611 RGO:21612 tricuspid stenosis with pulmonary stenosis RGO:21612 RGO:21615 total anomalous pulmonary venous return above the diaphragm RGO:21615 small ASD RGO:21616 small atrial septal defect RGO:21616 RGO:21617 small VSD RGO:21617 RGO:21618 small PDA RGO:21618 RGO:21619 small patent ductus arteriosus RGO:21619 acrocephalosyndactyly syndrome SNOMEDCT:268262006 RGO:21621 acrocephalosyndactyly RGO:21621 acrocephalosyndactyly Apert type DOID:12960 ORDO:87 RADLEX:RID35015 SNOMEDCT:205258009 RGO:21622 Apert syndrome RGO:21622 RGO:21624 IVC filter RGO:21624 RGO:21625 large atrioventricular canal defect RGO:21625 RGO:21629 tricuspid atresia with transposition of great vessels RGO:21629 RGO:21630 tricuspid stenosis with transposition of great vessels RGO:21630 RGO:21631 Potts procedure RGO:21631 RGO:21632 penetrating chest trauma RGO:21632 RGO:21633 normal finding in adult women under 25 RGO:21633 RGO:21634 pulmonary arterial disease RGO:21634 SNOMEDCT:128238001 RGO:21635 chronic heart disease RGO:21635 RGO:21636 diffuse lung disease RGO:21636 RGO:21637 corrected transposition with left-sided ascending aorta and PS RGO:21637 RGO:21638 chest trauma RGO:21638 DNL RGO:21639 diffuse necrotizing leukoencephalopathy RGO:21639 DOID:10579 HP:0002415 SNOMEDCT:192781003 RGO:21642 leukodystrophy RGO:21642 HP:0006685 RGO:21650 endocardial fibrosis RGO:21650 ORDO:99084 RGO:21653 pulmonary artery branch stenosis RGO:21653 RGO:21655 dissecting aneurysm of aorta RGO:21655 RGO:21656 medial necrosis of aorta RGO:21656 rhabdomyoma of heart HP:0009729 RGO:21659 cardiac rhabdomyoma RGO:21659 RGO:21661 hypoplasia of pulmonary arteries RGO:21661 RGO:21664 pericardial hernia RGO:21664 SNOMEDCT:445540004 RGO:21665 left ventricular diverticulum RGO:21665 HP:0011571 RADLEX:RID4794 RGO:21666 parachute mitral valve RGO:21666 fibroma of heart HP:0010617 RGO:21667 cardiac fibroma RGO:21667 SNOMEDCT:62185008 RGO:21670 pancarditis RGO:21670 RGO:21671 cystic medial necrosis of pulmonary artery RGO:21671 HP:0012722 SNOMEDCT:233916004 RGO:21672 heart block RGO:21672 DOID:1926 ICD10CM:E75.22 ORDO:355 RADLEX:RID34415 SNOMEDCT:190794006 RGO:21673 Gaucher disease RGO:21673 DOID:14504 ICD10CM:E75.24 SNOMEDCT:58459009 RGO:21674 Niemann-Pick disease RGO:21674 RGO:21675 persistence of left supracardinal vein RGO:21675 DOID:397 HP:0001723 RADLEX:RID3255 SNOMEDCT:415295002 RGO:21676 restrictive cardiomyopathy RGO:21676 HP:0004420 SNOMEDCT:65198009 RGO:21677 arterial thrombosis RGO:21677 RGO:21679 leiomyosarcoma of inferior vena cava RGO:21679 RGO:21680 angiosarcoma of inferior vena cava RGO:21680 RGO:21681 lipoma of inferior vena cava RGO:21681 RGO:21682 arteriovenous malformation of thoracic wall RGO:21682 RGO:21683 anatomically corrected malposition of great arteries RGO:21683 RGO:21687 transposition of great vessels with large VSD RGO:21687 RGO:21688 transposition of great vessels with large PDA RGO:21688 RGO:21689 mitral insufficiency RGO:21689 RADLEX:RID1825 SNOMEDCT:386639001 RGO:21690 abortion RGO:21690 RGO:21691 vaginal insufflation RGO:21691 SNOMEDCT:22484001 RGO:21692 cunnilingus RGO:21692 RADLEX:RID35814 SNOMEDCT:309849004 RGO:21694 pericardiocentesis RGO:21694 SNOMEDCT:89305009 RGO:21695 peritoneocentesis RGO:21695 RGO:21696 chronic spondylitis RGO:21696 RGO:21697 lipid granulomatosis RGO:21697 RGO:21698 notochordal remnant RGO:21698 RGO:21699 insufficiency fracture of sacrum RGO:21699 RGO:21700 nondiscogenic sclerosis RGO:21700 RGO:21701 traumatic vertebral osteonecrosis RGO:21701 osteonecrosis of vertebral body DOID:6603 RGO:21702 Kümmell disease RGO:21702 HP:0004610 RGO:21705 narrow lumbar spinal canal RGO:21705 HP:0004633 RGO:21706 lower thoracic kyphosis RGO:21706 HP:0002938 RGO:21707 lumbar lordosis RGO:21707 RGO:21709 massive hydronephrosis RGO:21709 RGO:21710 hemolytic disease RGO:21710 RGO:21711 gastrointestinal cyst RGO:21711 RGO:21713 maternal pelvic neoplasm RGO:21713 RGO:21714 maternal pelvic cyst RGO:21714 RGO:21715 distended maternal bladder RGO:21715 RGO:21716 distended maternal rectum RGO:21716 RGO:21717 maternal spondylolisthesis RGO:21717 RGO:21718 maternal ischial spine prominence RGO:21718 RGO:21719 maternal pelvic girdle deformity RGO:21719 RGO:21720 uterine malformation RGO:21720 RGO:21721 persistent uterine contraction ring RGO:21721 RGO:21722 umbilical cord twist RGO:21722 RGO:21723 umbilical cord shortening RGO:21723 RGO:21724 thrombosis of pelvic veins RGO:21724 RGO:21725 coagualtion disorder RGO:21725 osseous metastasis skeletal metastasis RGO:21726 bone metastasis RGO:21726 RGO:21727 primary spinal tumor RGO:21727 HP:0010618 ORDO:314473 RGO:21728 ovarian fibroma RGO:21728 DOID:5511 RGO:21729 ovarian dysgerminoma RGO:21729 RGO:21730 corpus albicans RGO:21730 RGO:21731 sclerosing stromal neoplasm RGO:21731 thickening of gallbladder wall RGO:21742 gallbladder wall thickening RGO:21742 RGO:21744 athletic conditioning RGO:21744 RGO:21745 idiopathic pneumopericardium RGO:21745 Andersen disease RGO:21746 glycogen storage disease type 4 RGO:21746 MPS 1 ORDO:579 RGO:21748 mucopolysaccharidosis type 1 RGO:21748 RGO:21759 large atrial septal defect with heart failure RGO:21759 RGO:21760 large ventricular septal defect with heart failure RGO:21760 RGO:21761 large patent ductus arteriosus with heart failure RGO:21761 large ASD RGO:21763 large atrial septal defect RGO:21763 RGO:21764 large patent ductus arteriosus RGO:21764 RGO:21769 complete transposition of great vessels and VSD without PS RGO:21769 RGO:21770 complete transposition of great vessels and PDA without PS RGO:21770 RGO:21771 corrected transposition of great vessels and VSD without PS RGO:21771 RGO:21772 corrected transposition of great vessels and PDA without PS RGO:21772 RGO:21773 corrected transposition with medially positioned pulmonary artery RGO:21773 RGO:21775 prosthetic aortic valve replacement RGO:21775 DOID:3393 HP:0001677 RGO:21776 coronary disease RGO:21776 RGO:21780 embolic metastases RGO:21780 ICD10CM:I50.1 SNOMEDCT:85232009 RGO:21781 left heart failure RGO:21781 RGO:21783 pulmonary hypertension with interatrial communication RGO:21783 RGO:21786 tracheal injury RGO:21786 RGO:21787 coarctation syndrome RGO:21787 RGO:21788 normal response to cold RGO:21788 SNOMEDCT:134296002 RGO:21789 paradoxical embolus RGO:21789 RGO:21790 metastatic disease to heart RGO:21790 SNOMEDCT:68444001 RGO:21791 adriamycin RGO:21791 SNOMEDCT:372817009 SNOMEDCT:68444001 RGO:21792 doxorubicin RGO:21792 HP:0001717 RADLEX:RID50146 RGO:21794 coronary artery calcification RGO:21794 beer drinker cardiomyopathy SNOMEDCT:50275009 RGO:21796 cobalt cardiomyopathy RGO:21796 SNOMEDCT:69463008 RGO:21801 Maroteaux-Lamy disease RGO:21801 SNOMEDCT:126071000 RGO:21802 ergonovine RGO:21802 levocardia with situs inversus SNOMEDCT:125254004 SNOMEDCT:134221003 RGO:21805 levoversion RGO:21805 RGO:21807 dextroposition RGO:21807 HP:0011599 ORDO:95443 SNOMEDCT:16567006 RGO:21808 mesocardia RGO:21808 RGO:21809 severe anemia RGO:21809 SNOMEDCT:445305001 RGO:21810 cavernous hemangioma of skin RGO:21810 SNOMEDCT:77334002 RGO:21811 sodium chloride poisoning RGO:21811 HP:0100784 RGO:21812 peripheral arteriovenous fistula RGO:21812 DOID:490 RGO:21813 pulmonary hemangioma RGO:21813 RGO:21814 anomalous left coronary from pulmonary artery RGO:21814 ORDO:99050 RGO:21818 pulmonary artery arising from aorta RGO:21818 RGO:21819 thoracic wall arteriovenous malformation RGO:21819 Blalock procedure Blalock-Thomas-Taussig shunt RADLEX:RID1566 SNOMEDCT:13662000 RGO:21820 Blalock-Taussig shunt RGO:21820 SNOMEDCT:126713003 RGO:21823 neoplasm of lung RGO:21823 RGO:21824 acrocephalosyndactyly Saethre-Chotzen type RGO:21824 HP:0010034 RGO:21826 short 1st metacarpal RGO:21826 SNOMEDCT:12377007 RGO:21827 increased central venous pressure RGO:21827 RGO:21830 neoplasm of thyroid RGO:21830 SNOMEDCT:126725000 RGO:21831 neoplasm of mediastinum RGO:21831 RGO:21832 paratracheal mass RGO:21832 RGO:21833 paratracheal cyst RGO:21833 RGO:21834 cystic abdominal mass RGO:21834 RGO:21836 distended stomach RGO:21836 RGO:21837 distended splenic flexure of colon RGO:21837 HP:0010047 RGO:21838 short 5th metacarpal RGO:21838 HP:0009778 RGO:21839 short thumb RGO:21839 RGO:21840 short great toe RGO:21840 RGO:21843 bone aplasia RGO:21843 RGO:21844 bone hypoplasia RGO:21844 RGO:21845 asymmetry of size of hand bones RGO:21845 flat feet flatfeet flatfoot HP:0001763 SNOMEDCT:53226007 RGO:21846 pes planus RGO:21846 HP:0001761 SNOMEDCT:249802001 RGO:21847 pes cavus RGO:21847 RGO:21848 everted feet RGO:21848 RGO:21849 pes valgus planus RGO:21849 RGO:21850 misshapen tarsals RGO:21850 RGO:21851 hypoplasia of sternum RGO:21851 RGO:21852 Erb palsy RGO:21852 RGO:21853 accessory diaphragm RGO:21853 SNOMEDCT:56110009 RGO:21854 birth trauma RGO:21854 RADLEX:RID5573 RGO:21855 chest tube RGO:21855 RGO:21857 subclavian vein puncture RGO:21857 DOID:1803 HP:0009830 SNOMEDCT:128192007 RGO:21858 peripheral neuritis RGO:21858 RGO:21859 maternal-fetal hemorrhage RGO:21859 RGO:21860 placental transfusion syndrome RGO:21860 RGO:21865 calcification of aortic annulus RGO:21865 RGO:21866 calcification of mitral annulus RGO:21866 SNOMEDCT:473372009 RGO:21867 calcification of mitral valve RGO:21867 RGO:21869 calcification of left atrial wall RGO:21869 RGO:21870 calcification of aortic valve RGO:21870 DOID:3393 SNOMEDCT:53741008 RGO:21871 coronary arteriosclerosis RGO:21871 RGO:21872 Mönckeberg sclerosis of coronary artery RGO:21872 SNOMEDCT:445512009 RGO:21873 calcification of coronary artery RGO:21873 medial calcific sclerosis RADLEX:RID3292 RGO:21874 Mönckeberg sclerosis RGO:21874 RGO:21876 severe gastric dilatation RGO:21876 RGO:21877 chronic hemothorax RGO:21877 SNOMEDCT:126728003 RGO:21878 neoplasm of diaphragm RGO:21878 RGO:21879 idiopathic diaphragmatic paralysis RGO:21879 RGO:21881 congenitally absent bronchus RGO:21881 RGO:21882 surgically absent bronchus RGO:21882 RADLEX:RID4227 SNOMEDCT:11671000 RGO:21883 adenoid cystic carcinoma RGO:21883 HP:0031024 SNOMEDCT:302827006 RGO:21884 cylindroma RGO:21884 RGO:21885 malpositioned endotracheal tube RGO:21885 RADLEX:RID4437 SNOMEDCT:12169001 SNOMEDCT:404035005 RGO:21886 granular cell myoblastoma RGO:21886 RGO:21887 enlarged left atrium RGO:21887 SNOMEDCT:42216004 RGO:21890 mucus plug RGO:21890 RGO:21891 obstructing neoplasm RGO:21891 RGO:21892 endobronchial metastasis RGO:21892 SNOMEDCT:40294009 RGO:21895 Paragonimus RGO:21895 RGO:21897 endobronchial neoplasm RGO:21897 RGO:21900 idiopathic mucoid impaction RGO:21900 RGO:21901 elderly female patient RGO:21901 fusiform bronchiectasis tubular bronchiectasis SNOMEDCT:83457000 RGO:21902 cylindrical bronchiectasis RGO:21902 RGO:21905 central bronchiectasis RGO:21905 cystic bronchiectasis SNOMEDCT:52500008 RGO:21906 saccular bronchiectasis RGO:21906 pseudobronchiectasis RGO:21907 reversible bronchiectasis RGO:21907 RADLEX:RID28528 SNOMEDCT:19325002 RGO:21909 traction bronchiectasis RGO:21909 ampullary bronchiectasis RGO:21910 varicose bronchiectasis RGO:21910 RGO:21912 metastasis to tracheal mucosa RGO:21912 RGO:21917 chronic lung abscess RGO:21917 RGO:21918 calcified pleural plaque RGO:21918 RGO:21920 asbestos pleural plaque RGO:21920 RGO:21921 rib callus RGO:21921 HP:0006646 RGO:21922 costal cartilage calcification RGO:21922 HP:0004380 SNOMEDCT:250978003 RGO:21923 aortic valve calcification RGO:21923 HP:0004382 RGO:21924 mitral valve calcification RGO:21924 SNOMEDCT:198009004 SNOMEDCT:2160002 RGO:21926 ligamentum arteriosum RGO:21926 ICD10CM:I25.2 SNOMEDCT:1755008 RGO:21927 old myocardial infarction RGO:21927 RGO:21928 intracardiac myxoma RGO:21928 RGO:21929 intracardiac thrombus RGO:21929 RGO:21930 breast neoplasm RGO:21930 RGO:21931 rib neoplasm RGO:21931 RGO:21932 chest wall neoplasm RGO:21932 RGO:21933 nonspecific calcified granuloma RGO:21933 SNOMEDCT:254643009 RGO:21934 intrapulmonary teratoma RGO:21934 RGO:21935 IVC thrombus RGO:21935 SVC thrombosis RGO:21936 superior vena cava thrombosis RGO:21936 RGO:21937 calcific pericarditis RGO:21937 RGO:21938 pulmonary varix RGO:21938 DOID:8622 ICD10CM:B05 SNOMEDCT:14189004 RGO:21940 measles RGO:21940 DOID:13166 ICD10CM:B44.81 ORDO:1164 RADLEX:RID34668 SNOMEDCT:37981002 RGO:21941 allergic bronchopulmonary aspergillosis RGO:21941 RGO:21942 inhalation of noxious fumes RGO:21942 ICD10CM:T59.81 RADLEX:RID4580 RGO:21943 smoke inhalation RGO:21943 RGO:21944 chemical inhalation RGO:21944 RGO:21945 bronchial stricture RGO:21945 SNOMEDCT:3304005 RGO:21946 bronchial compression RGO:21946 RGO:21947 post-stenotic constriction RGO:21947 RGO:21950 traumatic cartilage deficiency RGO:21950 RGO:21951 congenital cartilage deficiency RGO:21951 RGO:21952 chronic fibrosing mediastinitis RGO:21952 RGO:21953 saber-sheath trachea RGO:21953 DOID:0060313 ICD10CM:Q32.0 ORDO:95430 SNOMEDCT:95467005 RGO:21955 congenital tracheomalacia RGO:21955 HP:0011598 RGO:21956 right aortic arch with aberrant left subclavian artery RGO:21956 RGO:21957 Klebsiella rhinoscleromatis infection RGO:21957 DOID:3227 HP:0002777 SNOMEDCT:11296007 RGO:21960 tracheal stenosis RGO:21960 RGO:21961 chemical stricture RGO:21961 SNOMEDCT:13617004 RGO:21963 tracheobronchitis RGO:21963 SNOMEDCT:442110002 RGO:21964 pleural fibrosis RGO:21964 RGO:21965 right upper lobe atelectasis RGO:21965 DOID:5041 RADLEX:RID45696 SNOMEDCT:363402007 RGO:21966 esophageal cancer RGO:21966 RGO:21967 enlarged mediastinal lymph nodes RGO:21967 RGO:21968 mediastinal surgery RGO:21968 SNOMEDCT:261479009 RGO:21969 mediastinoscopy RGO:21969 RGO:21970 right radical neck dissection RGO:21970 RGO:21972 right vagus nerve schwannoma RGO:21972 RGO:21973 phrenic nerve schwannoma RGO:21973 RGO:21974 radiation edema RGO:21974 RGO:21976 dilated esophagus RGO:21976 RGO:21977 tracheal cyst RGO:21977 RGO:21978 extramedullary myeloma RGO:21978 HP:0100028 SNOMEDCT:214660000 RGO:21979 ectopic thyroid tissue RGO:21979 SNOMEDCT:254621001 RGO:21980 laryngotracheal papillomatosis RGO:21980 DOID:4531 RADLEX:RID4254 SNOMEDCT:4079000 RGO:21981 mucoepidermoid carcinoma RGO:21981 DOID:4231 HP:0012315 SNOMEDCT:128741006 SNOMEDCT:302843004 RGO:21983 histiocytoma RGO:21983 HP:0012118 SNOMEDCT:363429002 RGO:21985 laryngeal cancer RGO:21985 RGO:21986 staphylococcal abscesses RGO:21986 RGO:21988 blebs RGO:21988 RGO:21992 necrotic metastases RGO:21992 RGO:21993 pulmonary angiitis and granulomatosis RGO:21993 RADLEX:RID5345 SNOMEDCT:233749003 RGO:21995 progressive massive fibrosis RGO:21995 RGO:21996 primary multicentric lung carcinoma RGO:21996 PCP pneumocystosis DOID:11339 RGO:21998 Pneumocystis carinii pneumonia RGO:21998 VZV RGO:22001 varicella zoster virus RGO:22001 ICD10CM:T005 SNOMEDCT:49872002 SNOMEDCT:T005 RGO:22003 virus RGO:22003 SNOMEDCT:59674005 RGO:22005 Nocardia RGO:22005 SNOMEDCT:42625000 RGO:22007 Strongyloides stercoralis RGO:22007 SNOMEDCT:61949005 RGO:22008 Toxoplasma RGO:22008 SNOMEDCT:2429008 RGO:22011 Aspergillus RGO:22011 RGO:22012 mucormycetes RGO:22012 SNOMEDCT:3265006 RGO:22013 Candida RGO:22013 SNOMEDCT:17579001 RGO:22014 Cryptococcus RGO:22014 SNOMEDCT:3092008 RGO:22016 Staphylococcus aureus RGO:22016 SNOMEDCT:58800005 RGO:22017 Streptococcus RGO:22017 SNOMEDCT:7527002 RGO:22018 Legionella RGO:22018 SNOMEDCT:75032006 RGO:22019 Klebsiella RGO:22019 SNOMEDCT:113861009 RGO:22021 Mycobacterium tuberculosis RGO:22021 RGO:22022 Mycobacterium avium-intracellulare complex RGO:22022 RGO:22023 MAC RGO:22023 RGO:22024 coronary artery fistula to right heart RGO:22024 coronary artery fistula to pulmonary artery coronary-pulmonary artery fistula RGO:22026 coronary artery-pulmonary artery fistula RGO:22026 RGO:22027 pulmonary sequestration with azygous drainage RGO:22027 RGO:22028 rupture of aortic valve cusp with VSD RGO:22028 RGO:22029 rupture of aortic valve cusp into right atrium RGO:22029 RGO:22030 Waterston procedure RGO:22030 RGO:22031 pulmonary artery obstruction RGO:22031 RGO:22033 infection of chest wall RGO:22033 RGO:22036 renal cell carcinoma metastasis to lung RGO:22036 DOID:5262 RGO:22038 sarcoma of heart RGO:22038 DOID:14539 SNOMEDCT:94327000 RGO:22039 metastasis to heart RGO:22039 RGO:22042 sarcoma of pulmonary artery RGO:22042 RGO:22043 neoplasm of pulmonary artery RGO:22043 Gasul syndrome Gasul transformation RGO:22045 VSD with infundibular pulmonary stenosis RGO:22045 RGO:22047 obstruction of pulmonary vein RGO:22047 RGO:22048 granulomatous lung disease RGO:22048 RGO:22049 obstruction of pulmonary artery RGO:22049 RGO:22050 pulmonary vein thrombus RGO:22050 RGO:22052 pulmonary artery stenosis with post-stenotic dilatation RGO:22052 RGO:22053 occlusion of pulmonary artery RGO:22053 RGO:22054 surgical ligation of pulmonary artery RGO:22054 RGO:22055 invasive neoplasm RGO:22055 SNOMEDCT:126640008 RGO:22056 neoplasm of chest wall RGO:22056 RGO:22057 Hodgkin disease involving chest wall RGO:22057 ORDO:980 RGO:22058 absence of pulmonary artery RGO:22058 SNOMEDCT:14799000 SNOMEDCT:252986008 RGO:22059 tumor embolus RGO:22059 SNOMEDCT:392031002 RGO:22060 endarterectomy RGO:22060 RGO:22061 atheromatous plaque with mural thrombus RGO:22061 RGO:22062 atheromatous ulcer with mural thrombus RGO:22062 SNOMEDCT:51670003 RGO:22063 mural thrombus RGO:22063 RGO:22064 surgical ligation of IVC RGO:22064 RGO:22066 pelvic lymphocele RGO:22066 SNOMEDCT:77123007 RGO:22068 lymphedema praecox RGO:22068 RGO:22073 pneumoconiosis with conglomerate mass RGO:22073 SNOMEDCT:22625005 RGO:22075 mediastinal hematoma RGO:22075 ICD10CM:J43.0 SNOMEDCT:45145000 RGO:22079 unilateral emphysema RGO:22079 SNOMEDCT:108306002 RGO:22080 dental procedure RGO:22080 RGO:22081 enema perforation into vessel RGO:22081 DOID:752 RGO:22082 peptic ulcer perforation RGO:22082 RGO:22083 severe preductal coarctation of aorta RGO:22083 HP:0001998 SNOMEDCT:52767006 RGO:22084 neonatal hypoglycemia RGO:22084 RGO:22085 prenatal closure of foramen ovale RGO:22085 DOID:61 ICD10CM:I05.1 SNOMEDCT:31085000 RGO:22086 rheumatic mitral insufficiency RGO:22086 RGO:22087 left atrial neoplasm RGO:22087 RGO:22089 giant left atrium syndrome RGO:22089 RGO:22090 papillary muscle dysfunction RGO:22090 SNOMEDCT:253541009 RGO:22091 left ventricular dilatation RGO:22091 SNOMEDCT:42069006 RGO:22093 myxomatous degeneration of mitral valve RGO:22093 RGO:22094 anomaly of mitral annulus RGO:22094 RGO:22096 corrected transposition of great vessels with anomalous left atrioventricular valve RGO:22096 RGO:22097 traumatic pericarditis RGO:22097 DOID:1787 HP:0001701 ORDO:58208 RADLEX:RID3534 SNOMEDCT:3238004 RGO:22098 pericarditis RGO:22098 RGO:22099 fenestrated aortic valve RGO:22099 RGO:22101 aortic valvulitis RGO:22101 DOID:10314 HP:0100584 SNOMEDCT:56819008 RGO:22102 endocarditis RGO:22102 RGO:22103 rupture of aortic cusp RGO:22103 RGO:22106 thrombosis of prosthetic aortic valve RGO:22106 RGO:22107 dissecting sinus of Valsalva aneurysm RGO:22107 RGO:22108 traumatic sinus of Valsalva aneurysm RGO:22108 RGO:22109 mycotic sinus of Valsalva aneurysm RGO:22109 SNOMEDCT:15016005 RGO:22111 pyogenic pericarditis RGO:22111 ICD10CM:I30.1 RGO:22112 staphylococcal pericarditis RGO:22112 ICD10CM:I30.1 RGO:22113 pneumococcal pericarditis RGO:22113 ICD10CM:B33.23 ICD10CM:I30.1 SNOMEDCT:70189005 RGO:22114 viral pericarditis RGO:22114 RGO:22115 Coxsackie B pericarditis RGO:22115 RGO:22116 prolonged hemodialysis RGO:22116 RGO:22117 chest neoplasm RGO:22117 RGO:22118 metastasis to pericardium RGO:22118 RGO:22119 amebic liver abscess with rupture into pericardial sac RGO:22119 RGO:22120 amebic lung abscess with rupture into pericardial sac RGO:22120 SNOMEDCT:41739008 RGO:22121 infectious pericarditis RGO:22121 SNOMEDCT:233883000 RGO:22122 bacterial pericarditis RGO:22122 RGO:22123 amebic pericarditis RGO:22123 DOID:1588 HP:0001873 SNOMEDCT:302215000 RGO:22125 thrombocytopenia RGO:22125 DOID:2235 RGO:22126 hypoprothrombinemia RGO:22126 subsepsis allergica DOID:3047 RGO:22128 Wissler syndrome RGO:22128 metastasis from breast carcinoma metastatic breast cancer RGO:22133 breast cancer metastasis RGO:22133 DOID:5158 SNOMEDCT:126719004 RGO:22135 neoplasm of pleura RGO:22135 HP:0002616 SNOMEDCT:251036003 RGO:22136 aortic root dilatation RGO:22136 ICD10CM:I77.81 RGO:22138 aortic ectasia RGO:22138 RGO:22142 valvotomy RGO:22142 RGO:22144 truncus arteriosus with large left-to-right shunt RGO:22144 RGO:22145 dextrocardia with situs solitus RGO:22145 RGO:22146 dextrocardia with situs indeterminate RGO:22146 SNOMEDCT:49795001 RGO:22147 pneumonectomy RGO:22147 ICD10CM:J94.1 RGO:22148 fibrothorax RGO:22148 RGO:22150 tricuspid atresia and transposition of great vessels with no PS RGO:22150 RGO:22151 systemic artery-pulmonary artery shunt RGO:22151 SNOMEDCT:236059003 RGO:22154 traumatic diaphragmatic hernia RGO:22154 RGO:22155 neurogenic neoplasm RGO:22155 RGO:22156 amebic abscess RGO:22156 SNOMEDCT:196067009 RGO:22158 pleural abscess RGO:22158 RGO:22159 hepatic hernia RGO:22159 RGO:22160 localized diaphragmatic eventration RGO:22160 DOID:10480 HP:0009110 SNOMEDCT:34168003 RGO:22161 diaphragmatic eventration RGO:22161 RGO:22162 fibroma of diaphragm RGO:22162 RGO:22163 myoma of diaphragm RGO:22163 RGO:22164 cystic teratoma of diaphragm RGO:22164 RGO:22165 metastasis to diaphragm RGO:22165 RGO:22167 lung sequestration RGO:22167 DOID:10195 SNOMEDCT:2460001000004103 RGO:22168 lipoma of pleura RGO:22168 RGO:22169 liposarcoma of pleura RGO:22169 SNOMEDCT:127230005 RGO:22173 neoplasm of spleen RGO:22173 RGO:22174 subphrenic cyst RGO:22174 RGO:22175 atelectasis of upper lobe RGO:22175 RGO:22176 normal scalloping of diaphragm RGO:22176 cystosarcoma phyllodes RADLEX:RID4287 SNOMEDCT:71232009 RGO:22177 phyllodes tumor RGO:22177 DOID:5138 SNOMEDCT:75210008 RGO:22179 leiomyomatosis RGO:22179 RGO:22180 benign metastasizing leiomyoma RGO:22180 SNOMEDCT:128588008 SNOMEDCT:198914002 RGO:22182 anomalous pulmonary artery RGO:22182 RGO:22183 Waterston-Cooley shunt RGO:22183 RGO:22184 Potts-Smith shunt RGO:22184 RGO:22185 air alveologram RGO:22185 RGO:22186 air bronchiologram RGO:22186 drowned lung SNOMEDCT:371072008 RGO:22190 obstructive pneumonia RGO:22190 DOID:4926 RADLEX:RID4243 SNOMEDCT:373627005 RGO:22191 bronchioloalveolar carcinoma RGO:22191 RGO:22193 slowly-resolving pneumonia RGO:22193 RADLEX:RID28518 RGO:22194 organizing pneumonia RGO:22194 torulosis DOID:12053 ICD10CM:B45 ORDO:1546 SNOMEDCT:42386007 RGO:22195 cryptococcosis RGO:22195 DOID:0050595 DOID:8485 SNOMEDCT:76627001 RGO:22197 mucormycosis RGO:22197 RADLEX:RID4836 RGO:22199 septic embolism RGO:22199 DOID:1176 HP:0002109 RGO:22203 bronchial disease RGO:22203 RGO:22204 peribronchial thickening RGO:22204 DOID:8007 SNOMEDCT:254638002 RGO:22205 Pancoast tumor RGO:22205 RGO:22206 metastases to pleura RGO:22206 RGO:22207 benign ovarian fibroma RGO:22207 DOID:386 RADLEX:RID4608 RGO:22208 postpericardiotomy syndrome RGO:22208 RGO:22209 therapeutic avulsion of phrenic nerve RGO:22209 RGO:22210 therapeutic injection of phrenic nerve RGO:22210 HP:0100682 RGO:22216 tracheal atresia RGO:22216 RGO:22217 fetal hydrothorax RGO:22217 HP:0001591 RGO:22221 bell-shaped thorax RGO:22221 SNOMEDCT:126639006 RGO:22224 neoplasm of axilla RGO:22224 RGO:22227 metastasis from tumor of head and neck RGO:22227 DOID:13408 SNOMEDCT:94493005 RGO:22228 metastasis to pleura RGO:22228 RGO:22229 metastasis from carcinoma of prostate RGO:22229 RGO:22230 pleural plaques RGO:22230 RGO:22231 thoracic splenosis RGO:22231 RADLEX:RID3916 SNOMEDCT:65832009 RGO:22232 mesothelial cyst RGO:22232 RGO:22233 metastatis to pleura RGO:22233 RGO:22235 metastasis from osteosarcoma RGO:22235 RGO:22237 interlobar pleural fluid RGO:22237 RGO:22238 metastasis from carcinoma of lung RGO:22238 RGO:22239 metastasis from carcinoma of ovary RGO:22239 prostate cancer metastases RGO:22240 prostate cancer metastasis RGO:22240 RGO:22241 metastasis from carcinoma of kidney RGO:22241 RGO:22242 metastasis from carcinoma of gastrointestinal tract RGO:22242 RGO:22244 massive hydrothorax RGO:22244 RGO:22245 postpneumonectomy fibrothorax RGO:22245 RGO:22246 congenital diaphragmatic hernia RGO:22246 SNOMEDCT:278484009 RGO:22247 tropical pulmonary eosinophilia RGO:22247 SNOMEDCT:46970008 RGO:22248 Mycoplasma pneumonia RGO:22248 SNOMEDCT:22696000 SNOMEDCT:387125005 RGO:22249 hydralazine RGO:22249 Hamman-Rich syndrome DOID:2800 ICD10CM:J84.114 SNOMEDCT:35037009 RGO:22253 acute interstitial pneumonitis RGO:22253 hyperplastic thymus RGO:22255 thymic hyperplasia RGO:22255 RGO:22256 thymitis RGO:22256 SNOMEDCT:13154009 SNOMEDCT:387071000 RGO:22258 nitrogen mustard RGO:22258 DOID:5566 RADLEX:RID4322 SNOMEDCT:42717009 RGO:22259 mature teratoma RGO:22259 RGO:22260 normal fat RGO:22260 RGO:22261 intrapericardial fat RGO:22261 DOID:0060326 HP:0002475 SNOMEDCT:414667000 RGO:22262 myelomeningocele RGO:22262 DOID:5262 HP:0031350 RGO:22263 cardiac sarcoma RGO:22263 RGO:22264 mature hydatid cyst RGO:22264 RGO:22265 hernia of liver RGO:22265 DOID:1540 HP:0006780 ORDO:143 SNOMEDCT:255037004 RGO:22266 parathyroid carcinoma RGO:22266 RGO:22267 infectious spondylitis RGO:22267 RGO:22268 fracture of spine with hematoma RGO:22268 ICD10CM:I71.9 SNOMEDCT:26660001 RGO:22269 dilatation of aorta RGO:22269 RGO:22270 tortuosity of aorta RGO:22270 RGO:22271 normal thymic enlargement RGO:22271 RGO:22272 mediastinal hemorrhage RGO:22272 RGO:22273 paraspinal hemorrhage RGO:22273 RGO:22274 foregut cyst RGO:22274 substernal goiter RGO:22275 mediastinal goiter RGO:22275 RGO:22279 pulmonary hypovascularity RGO:22279 RGO:22282 cystic adenomatoid malformation of lung RGO:22282 SNOMEDCT:13671009 RGO:22283 congenital urethral stricture RGO:22283 RGO:22284 congenital vaginal fistula RGO:22284 HP:0001643 SNOMEDCT:253684002 SNOMEDCT:4432005 RGO:22286 ductus arteriosus RGO:22286 RGO:22287 ligamentum arteriosus RGO:22287 SNOMEDCT:68409003 RGO:22292 organized pneumonia RGO:22292 SNOMEDCT:195900001 RGO:22293 measles pneumonia RGO:22293 RGO:22294 old pleural empyema RGO:22294 RGO:22295 intrathoracic thyroid RGO:22295 Allgrove syndrome RGO:22297 achalasia-adrenal-alacrima syndrome RGO:22297 DOID:0080156 HP:0008244 SNOMEDCT:93235007 RGO:22299 congenital adrenal hypoplasia RGO:22299 RADLEX:RID1756 SNOMEDCT:31904001 RGO:22300 adrenalectomy RGO:22300 ORDO:361 RGO:22301 familial glucocorticoid deficiency RGO:22301 RGO:22302 polyglandular autoimmune disease RGO:22302 DOID:4479 HP:0008242 SNOMEDCT:77098009 RGO:22303 pseudohypoaldosteronism RGO:22303 ORDO:3239 RGO:22306 achalasia-deafness-vitiligo syndrome RGO:22306 RGO:22307 familial achalasia RGO:22307 RGO:22308 popliteal artery entrapment syndrome RGO:22308 DOID:2935 ICD10CM:E70.330 ORDO:167 SNOMEDCT:111396008 RGO:22312 Chédiak-Higashi syndrome RGO:22312 RGO:22315 Coombs-pos­itive hemolytic anemia RGO:22315 RGO:22316 familial thrombocytopenia RGO:22316 DOID:13133 ICD10CM:O14.2 SNOMEDCT:95605009 RGO:22318 HELLP syndrome RGO:22318 Moschcowitz disease TTP DOID:10772 ICD10CM:M31.1 ORDO:54057 SNOMEDCT:78129009 RGO:22325 thrombotic thrombocytopenic purpura RGO:22325 RGO:22329 Noonan phenotype RGO:22329 RGO:22330 polyvalvular heart anomaly RGO:22330 RGO:22337 familial supravalvular aortic stenosis RGO:22337 ORDO:1455 RGO:22338 familial coarctation of aorta RGO:22338 RGO:22342 severe blood loss RGO:22342 RGO:22345 pulmonary hyperinflation RGO:22345 RGO:22348 chromosome 5p- syndrome RGO:22348 RGO:22351 aplasia or hypoplasia of labia majora RGO:22351 ORDO:2095 SNOMEDCT:205800003 RGO:22353 Gorlin-Chaudhry-Moss syndrome RGO:22353 COFS syndrome Pena-Shokeir syndrome type 2 cerebrooculofacioskeletal syndrome SNOMEDCT:41283003 RGO:22357 cerebro-oculo-facio-skeletal syndrome RGO:22357 SNOMEDCT:253905000 RGO:22359 megalourethra RGO:22359 ORDO:3307 RGO:22360 tetrasomy 18p syndrome RGO:22360 ring chromosome 18 RGO:22363 chromosome 18 ring RGO:22363 hypertelorism Teebi type ORDO:1519 RGO:22364 Teebi hypertelorism syndrome RGO:22364 HP:0002085 ICD10CM:Q01.2 ORDO:268823 SNOMEDCT:42376006 RGO:22371 occipital encephalocele RGO:22371 RGO:22374 hypoplastic olives and pyramids of the medulla oblongata RGO:22374 RGO:22378 giant-cell arteritis RGO:22378 HP:0001519 SNOMEDCT:62250003 RGO:22380 dolichostenomelia RGO:22380 SNOMEDCT:1171000119108 RGO:22381 recurrent inguinal hernia RGO:22381 RGO:22382 dilated aortic root RGO:22382 RGO:22385 medial degeneration of aorta RGO:22385 RGO:22386 medial degeneration of pulmonary artery RGO:22386 DOID:5232 HP:0025578 RGO:22391 aortic valve prolapse RGO:22391 RGO:22392 conduction abnormality RGO:22392 SNOMEDCT:56675007 RGO:22393 acute heart failure RGO:22393 RGO:22394 atrioventricular conduction abnormality RGO:22394 RGO:22397 intimal thickening of coronary artery RGO:22397 RGO:22398 valvular dysfunction RGO:22398 RGO:22407 idiopathic acro-osteosclerosis RGO:22407 DOID:10717 SNOMEDCT:4089001 RGO:22408 meningococcemia RGO:22408 RGO:22409 radium injury RGO:22409 RGO:22410 severe psoriatic arthritis RGO:22410 RGO:22411 ergot reaction RGO:22411 SNOMEDCT:27551008 RGO:22412 constriction RGO:22412 DOID:13117 HP:0001818 ICD10CM:L03.0 SNOMEDCT:71906005 RGO:22413 paronychia RGO:22413 RGO:22414 congenital sensory neuropathy RGO:22414 DOID:5587 SNOMEDCT:111247001 RGO:22417 Volkmann contracture RGO:22417 RGO:22418 isolated absence of phalanx RGO:22418 RGO:22419 isolated hypoplasia of phalanx RGO:22419 RGO:22422 familial subaortic membrane RGO:22422 RADLEX:RID3269 SNOMEDCT:8074002 RGO:22424 floppy valve syndrome RGO:22424 RGO:22425 Heyde syndrome RGO:22425 RGO:22429 Takayasu syndrome RGO:22429 RGO:22432 aplasia cutis RGO:22432 RGO:22433 colonic polyps RGO:22433 Hennekam lymphangiectasia-lymphedema syndrome intestinal lymphagiectasia-lymphedema-mental retardation syndrome DOID:0060366 ORDO:2136 RGO:22434 Hennekam syndrome RGO:22434 DOID:1390 HP:0003563 RGO:22435 hypobetalipoproteinemia RGO:22435 ORDO:3189 RGO:22437 familial congenital pulmonary valvular stenosis RGO:22437 RGO:22440 pulmonary valve dysplasia syndrome RGO:22440 RGO:22441 thick pulmonary valve leaflets RGO:22441 HP:0004322 SNOMEDCT:237836003 RGO:22442 small stature RGO:22442 HP:0000286 RGO:22443 epicanthal folds RGO:22443 HP:0000369 ICD10CM:Q17.4 RGO:22444 low-set ears RGO:22444 HP:0010512 SNOMEDCT:12286000 RGO:22449 adrenal calcification RGO:22449 HP:0006559 RGO:22452 hepatic calcification RGO:22452 HP:0005213 RGO:22453 pancreatic calcification RGO:22453 calcification of spleen SNOMEDCT:442360003 RGO:22455 splenic calcification RGO:22455 DOID:3827 HP:0000776 ICD10CM:K44 RADLEX:RID4934 SNOMEDCT:39839004 RGO:22456 diaphragmatic hernia RGO:22456 RGO:22458 hepatosplenomegaly in a neonate RGO:22458 DOID:5082 HP:0001394 RADLEX:RID3822 RGO:22460 cirrhosis RGO:22460 fatty change in liver fatty infiltration of liver hepatic steatosis HP:0001397 RADLEX:RID5217 SNOMEDCT:197321007 RGO:22461 fatty liver RGO:22461 fibrosis of liver liver fibrosis HP:0001395 ICD10CM:K74.0 SNOMEDCT:62484002 RGO:22462 hepatic fibrosis RGO:22462 dysplasia of pancreas pancreas dysplasia HP:0005232 RGO:22464 pancreatic dysplasia RGO:22464 fat deposition in pancreas fatty deposition in pancreas fatty infiltration of pancreas fatty replacement of pancreas RGO:22465 fatty pancreas RGO:22465 DOID:2913 HP:0001735 ICD10CM:K85 SNOMEDCT:197456007 RGO:22466 acute pancreatitis RGO:22466 RGO:22467 pancreatitis in a child RGO:22467 HP:0012732 SNOMEDCT:33225004 RGO:22470 anorectal anomaly RGO:22470 RGO:22471 biliary system abnormality RGO:22471 DOID:0060180 HP:0002583 RADLEX:RID3421 SNOMEDCT:64226004 RGO:22473 colitis RGO:22473 HP:0010943 RGO:22475 echogenic fetal bowel RGO:22475 acquired esophageal narrowing acquired narrowing of esophagus RGO:22476 acquired esophageal stenosis RGO:22476 DOID:10485 HP:0002032 ORDO:1199 SNOMEDCT:26179002 RGO:22477 esophageal atresia RGO:22477 dysfunction of esophagus RGO:22478 esophageal dysfunction RGO:22478 rupture of esophagus RGO:22479 esophageal rupture RGO:22479 functional disorder of gastrointestinal system functional gastrointestinal disorder RGO:22481 gastrointestinal dysfunction RGO:22481 cholelithiasis gallstones RADLEX:RID4989 SNOMEDCT:235919008 SNOMEDCT:256896000 RGO:22482 gallstone RGO:22482 GI bleeding gastrointestinal bleeding gastrointestinal hemorrhage gastrointestinal system hemorrhage RGO:22483 gastrointestinal system bleeding RGO:22483 bowel obstruction DOID:8437 HP:0005214 SNOMEDCT:81060008 RGO:22484 intestinal obstruction RGO:22484 HP:0002024 RADLEX:RID5275 SNOMEDCT:32230006 RGO:22486 malabsorption RGO:22486 HP:0002566 RGO:22487 intestinal malrotation RGO:22487 RADLEX:RID5284 SNOMEDCT:206528005 RGO:22488 meconium plug RGO:22488 HP:0004388 ICD10CM:Q43.8 SNOMEDCT:18389004 RGO:22490 microcolon RGO:22490 HP:0100841 ICD10CM:Q40.2 SNOMEDCT:83714006 RGO:22491 microgastria RGO:22491 SNOMEDCT:47367009 RGO:22492 pancreatic exocrine insufficiency RGO:22492 DOID:10602 HP:0002570 SNOMEDCT:66187002 RGO:22494 steatorrhea RGO:22494 RGO:22495 gastrointestinal tract ulcer RGO:22495 DOID:2355 HP:0001903 SNOMEDCT:271737000 RGO:22496 anemia RGO:22496 bleeding diathesis bleeding disorder clotting disorder coagulopathy HP:0001892 SNOMEDCT:64779008 RGO:22497 bleeding tendency RGO:22497 DOID:999 HP:0001880 ICD10CM:D72.1 SNOMEDCT:386789004 RGO:22498 eosinophilia RGO:22498 hypercalcemic state DOID:12678 HP:0003072 ICD10CM:E83.52 SNOMEDCT:66931009 RGO:22499 hypercalcemia RGO:22499 HP:0003155 RGO:22500 hyperphosphatasemia RGO:22500 DOID:0050459 HP:0002905 SNOMEDCT:20165001 RGO:22501 hyperphosphatemia RGO:22501 HP:0002901 ICD10CM:E83.51 SNOMEDCT:5291005 RGO:22502 hypocalcemia RGO:22502 DOID:9993 HP:0001943 RADLEX:RID5354 SNOMEDCT:302866003 RGO:22503 hypoglycemia RGO:22503 DOID:4500 HP:0002900 ICD10CM:E87.6 SNOMEDCT:43339004 RGO:22504 hypokalemia RGO:22504 DOID:0050336 HP:0002148 SNOMEDCT:4996001 RGO:22505 hypophosphatemia RGO:22505 DOID:12450 HP:0001876 ICD10CM:D61.81 SNOMEDCT:127034005 RGO:22506 pancytopenia RGO:22506 DOID:8432 HP:0001901 SNOMEDCT:127062003 RGO:22507 polycythemia RGO:22507 aortic valvular disease DOID:62 SNOMEDCT:8722008 RGO:22509 aortic valve disease RGO:22509 SNOMEDCT:233981004 RGO:22510 arterial aneurysm RGO:22510 HP:0003207 RGO:22512 arterial calcification RGO:22512 RGO:22513 arterial dilatation RGO:22513 HP:0005294 RADLEX:RID3319 SNOMEDCT:233992003 SNOMEDCT:710864009 RGO:22514 arterial dissection RGO:22514 HP:0025324 SNOMEDCT:2929001 RGO:22515 arterial occlusion RGO:22515 HP:0025019 SNOMEDCT:46126003 RGO:22516 arterial rupture RGO:22516 elongated arteries tortuous arteries HP:0005116 RGO:22518 arterial tortuosity RGO:22518 DOID:1936 HP:0002621 ICD10CM:I70 RADLEX:RID39049 SNOMEDCT:38716007 RGO:22519 atherosclerosis RGO:22519 A-V fistula AV fistula AVF HP:0004947 RGO:22520 arteriovenous fistulas RGO:22520 RGO:22521 common origin of carotid arteries RGO:22521 SNOMEDCT:275520000 RGO:22522 claudication RGO:22522 aortic coarctation HP:0001680 ICD10CM:Q25.1 ORDO:1457 RADLEX:RID34589 SNOMEDCT:7305005 RGO:22523 coarctation of aorta RGO:22523 RGO:22524 coronary artery abnormality RGO:22524 HP:0000822 RGO:22526 systemic hypertension RGO:22526 RGO:22527 systemic hypotension RGO:22527 HP:0030880 SNOMEDCT:266261006 RGO:22528 Raynaud phenomenon RGO:22528 DOID:1929 HP:0004381 ICD10CM:Q25.3 ORDO:3193 RGO:22529 supravalvular aortic stenosis RGO:22529 blushes hot flashes RGO:22531 vasomotor symptoms RGO:22531 cardiac arrhythmia heart arrhythmia irregular heartbeat HP:0011675 SNOMEDCT:698247007 RGO:22532 arrhythmia RGO:22532 calcification of heart heart calcification RGO:22533 cardiac calcification RGO:22533 CHF cardiac failure congestive heart failure HP:0001635 ICD10CM:I50 RADLEX:RID34795 SNOMEDCT:84114007 RGO:22534 heart failure RGO:22534 RGO:22535 cardiac valve thickening RGO:22535 HP:0001640 ICD10CM:I51.7 SNOMEDCT:8186001 RGO:22537 cardiomegaly RGO:22537 small heart RGO:22540 microcardia RGO:22540 DOID:61 SNOMEDCT:11851006 RGO:22541 mitral valve disease RGO:22541 MI DOID:5844 HP:0001658 RADLEX:RID3236 SNOMEDCT:22298006 RGO:22542 myocardial infarction RGO:22542 HP:0002593 ORDO:36204 SNOMEDCT:197260007 RGO:22544 intestinal lymphangiectasia RGO:22544 DOID:4977 HP:0001004 RADLEX:RID49595 SNOMEDCT:234097001 SNOMEDCT:30213001 RGO:22545 lymphedema RGO:22545 RGO:22547 pulmonary artery calcification RGO:22547 PE pulmonary artery embolism pulmonary artery thromboembolism pulmonary artery thrombosis pulmonary thromboembolism DOID:9477 HP:0002204 ICD10CM:I26 RADLEX:RID4834 SNOMEDCT:59282003 RGO:22548 pulmonary embolism RGO:22548 HP:0004415 SNOMEDCT:95441000 RGO:22550 pulmonary artery stenosis RGO:22550 pulmonary arterial hypertension pulmonary artery hypertension DOID:6432 RADLEX:RID3299 SNOMEDCT:70995007 RGO:22551 pulmonary hypertension RGO:22551 RGO:22552 macular stains RGO:22552 DOID:1272 HP:0001009 RADLEX:RID3348 SNOMEDCT:112641009 RGO:22553 telangiectasia RGO:22553 RADLEX:RID3332 SNOMEDCT:32776006 SNOMEDCT:400159008 RGO:22554 vascular malformation RGO:22554 RGO:22556 venous dilatation RGO:22556 RGO:22557 venous anomaly RGO:22557 HP:0025322 SNOMEDCT:307221007 RGO:22558 venous occlusion RGO:22558 phlebothrombosis HP:0004936 RADLEX:RID39185 SNOMEDCT:111293003 RGO:22559 venous thrombosis RGO:22559 large adrenal gland RGO:22561 adrenal enlargement RGO:22561 gonadal hypoplasia hypogenitalism hypoplastic genitalia DOID:1924 HP:0000135 SNOMEDCT:48130008 RGO:22563 hypogonadism RGO:22563 DOID:14038 HP:0000826 ICD10CM:E30.1 SNOMEDCT:400179000 RGO:22565 precocious puberty RGO:22565 DOID:3765 SNOMEDCT:75164001 RGO:22566 pseudohermaphroditism RGO:22566 DM diabetes DOID:9351 HP:0000819 SNOMEDCT:73211009 RGO:22567 diabetes mellitus RGO:22567 DOID:13543 HP:0000843 RADLEX:RID34610 SNOMEDCT:66999008 RGO:22568 hyperparathyroidism RGO:22568 DOID:11199 HP:0000829 ICD10CM:E20 SNOMEDCT:36976004 RGO:22569 hypoparathyroidism RGO:22569 DOID:9409 HP:0000873 ICD10CM:E23.2 SNOMEDCT:15771004 RGO:22570 diabetes insipidus RGO:22570 DOID:2444 HP:0010514 SNOMEDCT:10649000 RGO:22571 hyperpituitarism RGO:22571 DOID:9406 HP:0040075 ICD10CM:E23.0 SNOMEDCT:74728003 RGO:22572 hypopituitarism RGO:22572 DOID:12176 HP:0000853 RADLEX:RID3797 SNOMEDCT:3716002 RGO:22573 goiter RGO:22573 SNOMEDCT:264580006 RGO:22574 thyroid dysfunction RGO:22574 HP:0000062 ICD10CM:Q56.4 SNOMEDCT:21321009 RGO:22575 ambiguous genitalia RGO:22575 contracted bladder small bladder RGO:22576 small urinary bladder RGO:22576 SNOMEDCT:40492006 RGO:22578 bladder dysfunction RGO:22578 bladder enlargement enlarged bladder large urinary bladder megacystis SNOMEDCT:300455006 RGO:22579 large bladder RGO:22579 calcification of bladder wall RGO:22580 bladder wall calcification RGO:22580 RGO:22581 scrotal calcification RGO:22581 large clitorus HP:0008665 SNOMEDCT:80212005 RGO:22583 clitoromegaly RGO:22583 DOID:11383 HP:0000028 SNOMEDCT:204878001 RGO:22584 cryptorchidism RGO:22584 RGO:22585 genital anomaly RGO:22585 HP:0002150 SNOMEDCT:71938000 RGO:22586 hypercalciuria RGO:22586 DOID:10892 HP:0000047 ICD10CM:Q54 SNOMEDCT:416010008 RGO:22587 hypospadias RGO:22587 HP:0000105 SNOMEDCT:300444006 RGO:22591 large kidney RGO:22591 SNOMEDCT:236448000 RGO:22592 small kidney RGO:22592 hypoplasia of labia majora HP:0000059 RGO:22593 hypoplastic labia majora RGO:22593 RGO:22594 male megalourethra RGO:22594 SNOMEDCT:88673001 RGO:22597 large penis RGO:22597 small penis HP:0000054 ICD10CM:Q55.62 SNOMEDCT:34911001 RGO:22598 micropenis RGO:22598 scrotomegaly RGO:22599 enlarged scrotum RGO:22599 HP:0000048 SNOMEDCT:236780002 RGO:22600 bifid scrotum RGO:22600 absent testes SNOMEDCT:371015003 RGO:22601 anorchia RGO:22601 RGO:22602 testicular anomaly RGO:22602 large testes macro-orchidism HP:0000053 RGO:22603 macroorchidism RGO:22603 RGO:22604 microorchidism RGO:22604 anomaly of uterus RGO:22605 uterine anomaly RGO:22605 RGO:22606 vaginal anomaly RGO:22606 HP:0000148 ORDO:65681 RGO:22607 vaginal atresia RGO:22607 RGO:22609 laryngeal anomaly RGO:22609 premature calcification of laryngeal cartilage RGO:22610 premature laryngeal cartilage calcification RGO:22610 agenesis of trachea ORDO:3346 RGO:22612 tracheal agenesis RGO:22612 primary tracheal stenosis ORDO:141127 RGO:22613 congenital tracheal stenosis x RGO:22613 RGO:22614 premature tracheobronchial cartilage calcification RGO:22614 RGO:22615 short trachea RGO:22615 DOID:0060313 HP:0002779 SNOMEDCT:95434006 RGO:22616 tracheomalacia RGO:22616 ORDO:3347 SNOMEDCT:57451009 RGO:22618 tracheobronchomegaly RGO:22618 RGO:22620 familial benign polycythemia RGO:22620 SNOMEDCT:234397008 RGO:22621 methemoglobin reductase deficiency RGO:22621 IgA deficiency SNOMEDCT:29260007 RGO:22623 immunoglobulin A deficiency RGO:22623 RGO:22624 somatostaninoma syndrome RGO:22624 RGO:22625 mesenteric metastasis RGO:22625 Goldberg syndrome galactosialidosis several forms ORDO:351 SNOMEDCT:35691006 RGO:22626 galactosialidosis RGO:22626 RGO:22627 corticosteroid therapy RGO:22627 HP:0005973 SNOMEDCT:20052008 RGO:22628 fructose intolerance RGO:22628 RGO:22629 lipoproteinemia RGO:22629 ORDO:42 RGO:22630 medium-chain acyl CoA dehydrogenase deficiency RGO:22630 SNOMEDCT:44047000 RGO:22631 Zieve syndrome RGO:22631 SNOMEDCT:88213004 RGO:22634 aldosteronism RGO:22634 RGO:22635 aldosteronoma RGO:22635 RGO:22636 intrauterine adrenal hemorrhage and necrosis RGO:22636 RGO:22637 autosomal recessive congenital diaphragmatic defects RGO:22637 RGO:22638 chromosome 8q22 translocation RGO:22638 RGO:22639 chromosome 9p- syndrome RGO:22639 RGO:22640 congenital complete bilateral agenesis of diaphragm RGO:22640 RGO:22641 tetrasomy 12p mosaicism RGO:22641 ICD10CM:G31.81 RGO:22643 Alpers disease RGO:22643 FIC1 deficiency PFIC1 progressive familial intrahepatic cholestasis type 1 RGO:22644 Byler disease RGO:22644 ORDO:172 RGO:22645 progressive familial intrahepatic cholestasis RGO:22645 RGO:22646 watery stools RGO:22646 DOID:423 HP:0003198 SNOMEDCT:129565002 RGO:22649 myopathy RGO:22649 DOID:936 HP:0001298 RADLEX:RID5055 SNOMEDCT:81308009 RGO:22650 encephalopathy RGO:22650 SNOMEDCT:88518009 RGO:22651 hepatocerebral degeneration RGO:22651 SNOMEDCT:127012008 RGO:22652 lipodystrophic diabetes RGO:22652 RGO:22653 odontomas-esophageal stenosis-liver cirrhosis syndrome RGO:22653 RGO:22654 pancreatic hyposecretion RGO:22654 RGO:22655 pulmonary diffusion defect RGO:22655 RGO:22656 rheumatoid disorder RGO:22656 RGO:22658 Weber-Christian syndrome RGO:22658 RGO:22659 acrodysplasia RGO:22659 DOID:10584 HP:0000510 ICD10CM:H35.52 ORDO:791 SNOMEDCT:28835009 RGO:22660 retinitis pigmentosa RGO:22660 DOID:1442 ORDO:726 RGO:22661 Alpers syndrome RGO:22661 SNOMEDCT:82949000 RGO:22668 agenesis of pancreas RGO:22668 RGO:22672 cervical lymphocele RGO:22672 RGO:22674 short gut RGO:22674 RGO:22675 familial renal-hepatic-pancreatic dysplasia RGO:22675 ORDO:233 SNOMEDCT:60318001 RGO:22681 Duane syndrome RGO:22681 RGO:22682 familial anorectal malformation RGO:22682 RGO:22683 familial imperforate anus, cleft lip, and iris coloboma RGO:22683 ORDO:2369 SNOMEDCT:716106000 RGO:22685 limb body wall complex RGO:22685 DOID:10488 HP:0002023 SNOMEDCT:204712000 RGO:22686 anal atresia RGO:22686 RGO:22687 abdominal placental attachment RGO:22687 RGO:22688 OEIS complex RGO:22688 RGO:22689 spinal defect RGO:22689 RGO:22690 persisting mesonephric duct syndrome RGO:22690 RGO:22693 polyoligodactyly RGO:22693 SGFLD RGO:22696 splenogonadal fusion-limb deformity syndrome RGO:22696 ORDO:3326 RGO:22697 thymic-renal-anal-lung dysplasia RGO:22697 ORDO:2881 RGO:22704 familial cutaneous photosensitivity and colitis RGO:22704 DOID:3753 ICD10CM:E70.331 ORDO:79430 SNOMEDCT:9311003 RGO:22705 Hermansky-Pudlak syndrome RGO:22705 RGO:22706 hypoalbuminemic state RGO:22706 DOID:0050450 ORDO:358 SNOMEDCT:707756004 RGO:22710 Gitelman syndrome RGO:22710 RGO:22712 VIPoma syndrome RGO:22712 HP:0002917 ICD10CM:E83.42 SNOMEDCT:190855004 RGO:22713 hypomagnesemia RGO:22713 HP:0003127 SNOMEDCT:86353007 RGO:22714 hypocalciuria RGO:22714 RGO:22716 cancer-related hypercalcemia RGO:22716 RGO:22717 diuretic phase of acute renal failure RGO:22717 DOID:0060699 ICD10CM:E83.52 ORDO:405 SNOMEDCT:237885008 RGO:22718 familial hypocalciuric hypercalcemia RGO:22718 HP:0008250 SNOMEDCT:276645004 RGO:22719 infantile hypercalcemia RGO:22719 RGO:22724 thiazide diuretics RGO:22724 RGO:22725 vitamin A intoxication RGO:22725 DOID:1338 HP:0004810 ICD10CM:D64.4 ORDO:293830 ORDO:85 SNOMEDCT:52951008 RGO:22726 congenital dyserythropoietic anemia RGO:22726 HP:0001071 RGO:22730 Fabry syndrome RGO:22730 DOID:2859 ORDO:2132 SNOMEDCT:51053007 RGO:22731 hemoglobin C disease RGO:22731 RGO:22733 hereditary nonspherocytic anemia RGO:22733 ICD10CM:D64.0 SNOMEDCT:62677000 RGO:22734 hereditary sideroblastic anemia RGO:22734 hyperostosis hyperphosphatemia syndrome RGO:22735 hyperostosis-hyperphosphatemia syndrome RGO:22735 RGO:22736 hyperphosphatasia-erythroblastopenia of childhood RGO:22736 Gräsbeck-Imerslund disease Imerslund-Najman-Gräsbeck syndrome familial megaloblastic anemia DOID:13382 ORDO:35858 SNOMEDCT:234363001 RGO:22737 Imerslund-Gräsbeck syndrome RGO:22737 RGO:22738 hereditary selective malabsorption of vitamin B12 RGO:22738 DOID:576 HP:0000093 ICD10CM:R80 RADLEX:RID5310 SNOMEDCT:29738008 RGO:22739 proteinuria RGO:22739 RGO:22741 lead intoxication RGO:22741 DOID:0050908 HP:0002863 ORDO:52688 SNOMEDCT:109995007 SNOMEDCT:128623006 RGO:22743 myelodysplastic syndrome RGO:22743 DOID:0060067 ORDO:699 SNOMEDCT:237985009 RGO:22745 Pearson syndrome RGO:22745 geophagia syndrome RGO:22746 Prasad syndrome RGO:22746 ICD10CM:H35.02 ORDO:190 RGO:22752 Coats retinopathy RGO:22752 RGO:22753 stagnant small-bowel syndrome RGO:22753 DOID:0050818 ICD10CM:D51.2 ORDO:859 SNOMEDCT:237934001 RGO:22754 transcobalamin II deficiency RGO:22754 DOID:10257 HP:0004905 ICD10CM:E50 SNOMEDCT:72000004 RGO:22755 vitamin A deficiency RGO:22755 RGO:22757 Waldenström syndrome RGO:22757 ICD10CM:D82.3 ORDO:2442 RGO:22759 X-linked lymphoproliferative disease RGO:22759 RGO:22760 congenital bilateral nerve deafness RGO:22760 RGO:22761 prolonged Q-T interval RGO:22761 RGO:22762 syncopal attacks RGO:22762 DOID:11759 HP:0001931 SNOMEDCT:44452003 RGO:22763 hypochromic anemia RGO:22763 RGO:22764 radioulnar defect RGO:22764 fructose-1,6-bisphosphatase deficiency DOID:5204 ORDO:348 SNOMEDCT:28183005 RGO:22767 fructose-1,6-diphosphatase deficiency RGO:22767 DOID:2018 SNOMEDCT:83469008 RGO:22770 hyperinsulinism RGO:22770 RGO:22771 islet cell dysplasia RGO:22771 SNOMEDCT:38196001 RGO:22772 Laron dwarfism RGO:22772 SNOMEDCT:76345009 RGO:22774 nesidioblastoma RGO:22774 HP:0001254 ICD10CM:R53.83 SNOMEDCT:214264003 RGO:22777 lethargy RGO:22777 HP:0001259 ICD10CM:R40.2 SNOMEDCT:371632003 RGO:22779 coma RGO:22779 RGO:22780 intrathoracic tumor RGO:22780 gallstome impacted in duodenal bulb RADLEX:RID4966 SNOMEDCT:431931000124108 RGO:22781 Bouveret syndrome RGO:22781 RGO:22784 abdominal cocoon syndrome RGO:22784 RGO:22785 absent intestinal musculature RGO:22785 SNOMEDCT:28212002 RGO:22786 brown bowel syndrome RGO:22786 RGO:22787 familial duodenal atresia RGO:22787 ORDO:2300 RGO:22790 familial intestinal atresia RGO:22790 SNOMEDCT:17186003 RGO:22791 ileocolic intussusception RGO:22791 ORDO:2538 RGO:22798 microgastria-limb reduction complex RGO:22798 RGO:22799 maternal hypermagnesemia RGO:22799 RGO:22800 postnatal hypermagnesemia RGO:22800 DOID:1386 HP:0008181 ICD10CM:E78.6 ORDO:14 SNOMEDCT:190787008 RGO:22803 abetalipoproteinemia RGO:22803 RGO:22804 somatostatinoma syndrome RGO:22804 RGO:22805 diverticulosis of jejunum RGO:22805 DOID:2361 HP:0001972 SNOMEDCT:83414005 RGO:22806 macrocytic anemia RGO:22806 RGO:22808 bone metastases RGO:22808 RGO:22811 major liver resection RGO:22811 SNOMEDCT:419933005 RGO:22812 glucocorticoid RGO:22812 RGO:22814 rapid mineralization RGO:22814 HP:0001950 ICD10CM:E87.3 SNOMEDCT:111378004 RGO:22815 respiratory alkalosis RGO:22815 SNOMEDCT:63722008 RGO:22816 chronic vomiting RGO:22816 RGO:22817 antacid medication RGO:22817 HP:0000938 RADLEX:RID5388 SNOMEDCT:312894000 SNOMEDCT:78441005 RGO:22818 osteopenia RGO:22818 RGO:22819 bone expansion RGO:22819 RGO:22820 ground-glass appearance RGO:22820 SNOMEDCT:201340008 RGO:22821 pigmented skin lesion RGO:22821 RGO:22822 allergic disorder RGO:22822 DOID:9502 SNOMEDCT:233692000 RGO:22823 cryptogenic pulmonary eosinophilia RGO:22823 DOID:998 ORDO:2582 RGO:22824 eosinophilia-myalgia syndrome RGO:22824 SNOMEDCT:79336007 RGO:22825 familial eosinophilia RGO:22825 DOID:612 RGO:22827 immune deficiency disorder RGO:22827 acute idiopathic eosinophilic pneumonia RGO:22828 Löffler syndrome RGO:22828 DOID:0060010 ORDO:39041 RGO:22829 Omenn syndrome RGO:22829 RGO:22830 parasitic infestation RGO:22830 RGO:22831 posttraumatic pleural effusion RGO:22831 DOID:8505 ICD10CM:L13.0 ORDO:1656 SNOMEDCT:111196000 RGO:22835 dermatitis herpetiformis RGO:22835 DOID:8893 HP:0003765 ICD10CM:L40 RADLEX:RID34691 SNOMEDCT:9014002 RGO:22837 psoriasis RGO:22837 RGO:22840 transient hyperphosphatemia of infancy RGO:22840 DOID:205 HP:0100774 SNOMEDCT:13814009 RGO:22841 hyperostosis RGO:22841 transient hyperphosphatasemia of infancy RGO:22846 idiopathic hyperphosphatasemia of childhood RGO:22846 RGO:22847 osteosclerotic metaphyseal dysplasia RGO:22847 RGO:22848 hyperphosphatasemia-erythroblastopenia of childhood RGO:22848 RGO:22849 familial hyperphosphatasia RGO:22849 RGO:22855 hemorrhagic shock-encephalopathy syndrome RGO:22855 DOID:2236 ICD10CM:D68.2 ORDO:98880 SNOMEDCT:154818001 RGO:22859 congenital afibrinogenemia RGO:22859 ORDO:79 RGO:22860 alpha2-antiplasmin deficiency RGO:22860 RGO:22861 idiopathic putmonary hemosiderosis RGO:22861 DOID:12531 ORDO:903 SNOMEDCT:128105004 RGO:22863 von Willebrand disease RGO:22863 RGO:22865 thrombocytopathia RGO:22865 HP:0003750 SNOMEDCT:80449002 RGO:22866 muscle fatigue RGO:22866 HP:0000616 ICD10CM:H57.03 SNOMEDCT:301939004 RGO:22867 miosis RGO:22867 DOID:4428 HP:0010522 SNOMEDCT:59770006 RGO:22868 dyslexia RGO:22868 DOID:0050449 SNOMEDCT:39427000 RGO:22873 Jadassohn-Lewandowsky syndrome RGO:22873 SNOMEDCT:253789002 RGO:22875 familial intestinal malrotation RGO:22875 RGO:22876 familial pancreatic enzyme insufficiency RGO:22876 ORDO:2069 RGO:22877 gastrocutaneous syndrome RGO:22877 RGO:22880 enterolithiasis RGO:22880 DOID:0060126 RGO:22884 alpha chain disease RGO:22884 SNOMEDCT:702364003 RGO:22885 Anderson syndrome RGO:22885 SNOMEDCT:396331005 RGO:22886 celiac syndrome RGO:22886 ORDO:47 SNOMEDCT:65880007 RGO:22888 X-linked agammaglobulinemia RGO:22888 HP:0002028 SNOMEDCT:236071009 RGO:22889 chronic diarrhea RGO:22889 RGO:22890 lipofuscin deposition in intestinal smooth muscle RGO:22890 HP:0001510 RADLEX:RID3805 SNOMEDCT:444896005 SNOMEDCT:59576002 RGO:22891 growth retardation RGO:22891 RGO:22892 transient neutropenia RGO:22892 DOID:8439 ICD10CM:K91.1 SNOMEDCT:80193009 RGO:22898 postgastrectomy syndrome RGO:22898 RGO:22899 stagnant small intestine syndrome RGO:22899 RGO:22900 diverticulosis of jejunum-macrocytic anemia-steatorrhea syndrome RGO:22900 ciliary dyskinesia dyskinetic cilia syndrome primary ciliary dyskinesia SNOMEDCT:86204009 RGO:22903 immotile cilia syndrome RGO:22903 RGO:22905 cerebrocostomandibular dysplasia RGO:22905 SNOMEDCT:51409009 RGO:22906 asymmetric crying facies RGO:22906 RGO:22913 mesobrachyphalangy RGO:22913 HP:0010778 RGO:22914 tracheomegaly RGO:22914 HP:0010777 RGO:22915 bronchomegaly RGO:22915 RGO:22916 chronic cigarette smoking RGO:22916 RGO:22918 marfanoid features RGO:22918 RGO:22919 tracheomegaly-bronchiectasis association RGO:22919 RGO:22920 brevicollis RGO:22920 RGO:22921 congenital cardiovascular disease RGO:22921 Nager syndrome DOID:5768 RGO:22923 Nager acrofacial dysostosis RGO:22923 RGO:22925 Möbius sequence RGO:22925 ORDO:2373 RGO:22927 autosomal dominant congenital laryngomalacia RGO:22927 Ortner syndrome RGO:22928 cardiovocal syndrome RGO:22928 HP:0001602 RGO:22932 laryngeal stenosis RGO:22932 RGO:22933 large echogenic lungs RGO:22933 RGO:22934 inverted diaphragm RGO:22934 RGO:22935 dilated distal airway RGO:22935 ORDO:2808 RGO:22936 familial congenital laryngeal abductor paralysis RGO:22936 RGO:22937 familial congenital partial atresia of larynx RGO:22937 RGO:22946 idiopathic infantile hypercalcemia RGO:22946 RGO:22950 warfarin sodium therapy RGO:22950 RGO:22951 acrocephalospondylosyndactyly RGO:22951 ORDO:2189 RGO:22955 hydrolethalus RGO:22955 DOID:14705 ORDO:710 SNOMEDCT:70410008 RGO:22956 Pfeiffer syndrome RGO:22956 ALPS autoimmune lymphoproliferative syndrome DOID:6688 SNOMEDCT:702444009 RGO:22957 Canale-Smith syndrome RGO:22957 RGO:22958 interruption of aortic arch with VSD RGO:22958 RGO:22959 interruption of aortic arch with PDA RGO:22959 HP:0004762 RADLEX:RID34741 SNOMEDCT:2829000 RGO:22960 hypoplasia of right ventricle RGO:22960 Ruvalcaba syndrome trichorhinophalangeal syndrome type 3 RGO:22962 trichorhinophalangeal dysplasia type 3 RGO:22962 RGO:22965 autosomal dominant ventricular tachycardia RGO:22965 ICD10CM:G90.01 SNOMEDCT:51723007 RGO:22966 carotid sinus syndrome RGO:22966 DOID:705 ORDO:104 SNOMEDCT:58610003 RGO:22970 Leber hereditary optic neuropathy RGO:22970 DOID:2843 ORDO:101016 SNOMEDCT:20852007 RGO:22971 Romano-Ward syndrome RGO:22971 DOID:13884 HP:0011704 ICD10CM:I49.5 SNOMEDCT:36083008 RGO:22972 sick sinus syndrome RGO:22972 ICD10CM:I45.9 SNOMEDCT:46935006 RGO:22973 Stokes-Adams syndrome RGO:22973 RGO:22974 syndrome X RGO:22974 WPW WPW syndrome RGO:22976 Wolf-Parkinson-White syndrome RGO:22976 SNOMEDCT:4554005 RGO:22980 intraventricular conduction defect RGO:22980 RGO:22981 bilateral loss of central vision RGO:22981 HP:0001279 SNOMEDCT:271594007 RGO:22982 syncope RGO:22982 RGO:22983 ventricular arrythmia RGO:22983 DOID:0050644 ORDO:51608 RGO:22984 arterial calcification of infancy RGO:22984 RGO:22985 Burger disease RGO:22985 GSD type 1 von Gierke disease RGO:22986 glycogen storage disease type 1 RGO:22986 DOID:11582 ICD10CM:A52.02 SNOMEDCT:20735004 RGO:22991 Syphilitic aortitis RGO:22991 SNOMEDCT:12694001 RGO:22993 anterior tibial compartment syndrome RGO:22993 RGO:22994 autosomal dominant supravalvular aortic stenosis RGO:22994 RGO:22995 blue digit syndrome RGO:22995 RGO:22997 Degos syndrome RGO:22997 SNOMEDCT:444744001 RGO:22998 hypothenar hammer syndrome RGO:22998 RGO:23001 quadrilateral space syndrome RGO:23001 PICA syndrome lateral medullary syndrome posterior inferior cerebellar artery syndrome DOID:3522 ICD10CM:G46.3 RGO:23003 Wallenberg syndrome RGO:23003 RGO:23004 esophageal atresia-tracheoesophageal fistula RGO:23004 DOID:0060562 RGO:23005 Bland-White-Garland syndrome RGO:23005 ORDO:95491 RGO:23006 congenital coronary artery aneurysm RGO:23006 SNOMEDCT:11433004 RGO:23007 congenital coronary artery fistula RGO:23007 RGO:23008 anomalous origin of the left coronary artery from the pulmonary artery RGO:23008 RGO:23015 postcoarctectomy syndrome RGO:23015 RGO:23017 brachymetacarpalia RGO:23017 RGO:23018 Addison syndrome RGO:23018 SNOMEDCT:56572001 RGO:23019 cyclic edema RGO:23019 RGO:23020 Muirhead syndrome RGO:23020 HP:0030005 ORDO:188 RGO:23021 systemic capillary leak syndrome RGO:23021 RGO:23022 hemoconcentration RGO:23022 HP:0007430 ICD10CM:R60.1 SNOMEDCT:16740003 SNOMEDCT:442433009 RGO:23023 generalized edema RGO:23023 RGO:23024 lgG paraprotein RGO:23024 DOID:11486 HP:0002277 SNOMEDCT:271730003 RGO:23025 Horner syndrome RGO:23025 RSD Sudeck atrophy complex regional pain syndrome type 1 DOID:1811 ICD10CM:G90.5 RGO:23026 reflex sympathetic dystrophy RGO:23026 idiopathic hypereosinophilia ORDO:3260 SNOMEDCT:414450004 SNOMEDCT:423294001 RGO:23030 idiopathic hypereosinophilic syndrome RGO:23030 HP:0010954 RGO:23031 hypoplastic right heart complex RGO:23031 mucopolysaccharidosis type 1H/1S RGO:23033 mucopolysaccharidosis type 1-H/S RGO:23033 MPS 1-S MPS I S Scheie disease Scheie syndrome mucopolysaccharidosis type I S mucopolysaccharidosis type I-S RGO:23034 mucopolysaccharidosis type 1-S RGO:23034 DOID:386 ICD10CM:I97.0 SNOMEDCT:78643003 RGO:23035 postcardiotomy syndrome RGO:23035 Meyenburg-Altherr-Uehlinger syndrome atrophic polychondritis chronic atrophic polychondritis systemic chondromalacia von Meyenburg disease DOID:2556 ICD10CM:M94.1 ORDO:728 RADLEX:RID5385 SNOMEDCT:72275000 RGO:23036 relapsing polychondritis RGO:23036 RGO:23039 viral pancreatitis RGO:23039 DOID:8568 RGO:23040 mononucleosis RGO:23040 RGO:23041 congestive liver disease RGO:23041 RGO:23042 colloidal gold therapy RGO:23042 SNOMEDCT:51040009 RGO:23043 thallium poisoning RGO:23043 African iron overload DOID:0111033 SNOMEDCT:66576001 RGO:23044 Bantu siderosis RGO:23044 RADLEX:RID3468 SNOMEDCT:442191002 RGO:23046 steatohepatitis RGO:23046 RGO:23047 vaculoar degeneration RGO:23047 SNOMEDCT:609302002 RGO:23051 pericardial cyst RGO:23051 RGO:23052 Storm syndrome RGO:23052 heart valve calcification valve calcification RGO:23053 valvular calcification RGO:23053 HP:0006698 ICD10CM:I25.3 SNOMEDCT:90539001 RGO:23054 ventricular aneurysm RGO:23054 HP:0002216 RGO:23057 premature graying RGO:23057 RGO:23058 premature hair loss RGO:23058 RGO:23059 myxomatous valvular degeneration RGO:23059 RGO:23060 cardiac valvular calcification RGO:23060 RGO:23061 valvular stenosis RGO:23061 embryonic testicular regression RGO:23063 familial anorchia RGO:23063 RGO:23065 adrenal rests RGO:23065 ORDO:1193 RGO:23066 Atkin-Flaitz syndrome RGO:23066 RGO:23067 benign idiopathic macroorchidism RGO:23067 RGO:23068 growth hormone treatment RGO:23068 DOID:2998 HP:0010788 RGO:23071 testicular tumor RGO:23071 ORDO:242 RGO:23076 chromosome XY gonadal dysgenesis RGO:23076 SNOMEDCT:414673004 RGO:23077 De Sanctis-Cacchione syndrome RGO:23077 multiple testes supernumary testes HP:0010470 SNOMEDCT:17471001 RGO:23079 polyorchidism RGO:23079 RGO:23080 rudimentary testes with Leydig cell deficiency RGO:23080 DOID:0050646 HP:0002804 ICD10CM:Q74.3 ORDO:1037 SNOMEDCT:77016009 RGO:23085 arthrogryposis multiplex congenita RGO:23085 RGO:23090 microgenitalism RGO:23090 HP:0004442 SNOMEDCT:109418001 RGO:23092 sagittal craniosynostosis RGO:23092 RGO:23093 mandibular ankylosis RGO:23093 HP:0030260 SNOMEDCT:276333003 SNOMEDCT:4801002 RGO:23094 microphallus RGO:23094 Sakati-Nyhan syndrome Sakati-Nyhan-Tisdale syndrome acrocephalopolysyndactyly type 3 ORDO:3128 RGO:23095 Sakati syndrome RGO:23095 ORDO:3338 RGO:23096 Toriello-Carey syndrome RGO:23096 RGO:23098 idiopathic megalourethra RGO:23098 penile megacyst RGO:23099 megacyst of the penis RGO:23099 RGO:23100 distal urethral obstruction RGO:23100 RGO:23106 branchiogenitoskeletal syndrome RGO:23106 DOID:0050769 ORDO:2608 RGO:23109 N syndrome RGO:23109 HP:0009803 RGO:23111 phalangeal hypoplasia RGO:23111 HP:0001798 ICD10CM:Q84.3 SNOMEDCT:23610003 RGO:23112 anonychia RGO:23112 RGO:23113 genital hypoplasia RGO:23113 RGO:23117 cerebro-oculofacioskeletal syndrome RGO:23117 HP:0001989 RGO:23118 fetal akinesia sequence RGO:23118 ORDO:2145 RGO:23120 Herrmann-Opitz syndrome RGO:23120 DOID:0050791 ORDO:2856 SNOMEDCT:702358005 RGO:23121 persistent müllerian duct syndrome RGO:23121 DOID:14768 ORDO:794 SNOMEDCT:83015004 RGO:23122 Saethre-Chotzen syndrome RGO:23122 ORDO:93974 RGO:23124 Smith-Fineman-Myers syndrome RGO:23124 DOID:4674 SNOMEDCT:52832001 RGO:23125 testicular feminization RGO:23125 Ochoa syndrome DOID:0050816 RGO:23126 urofacial syndrome RGO:23126 DOID:0060260 HP:0000508 RGO:23127 ptosis of eyelids RGO:23127 DOID:540 HP:0000486 SNOMEDCT:22066006 RGO:23128 strabismus RGO:23128 RGO:23129 partial agenesis of abdominal musculature RGO:23129 HP:0001385 RGO:23130 hip dysplasia RGO:23130 HP:0000324 SNOMEDCT:15253005 RGO:23132 facial asymmetry RGO:23132 HP:0010562 RGO:23133 keloids RGO:23133 HP:0000110 ICD10CM:Q61.4 ORDO:93108 SNOMEDCT:204949001 RGO:23134 renal dysplasia RGO:23134 HP:0001019 SNOMEDCT:399992009 RGO:23135 erythroderma RGO:23135 RGO:23136 sensory deafness RGO:23136 ORDO:84085 SNOMEDCT:429233001 RGO:23138 Hinman syndrome RGO:23138 ORDO:238637 SNOMEDCT:253904001 RGO:23139 megacystis-megaureter syndrome RGO:23139 RGO:23140 psychogenic retention syndrome RGO:23140 RGO:23141 urethral hypoplasia RGO:23141 ORDO:386 RGO:23148 cystic liver mesenchymal hamartoma RGO:23148 RGO:23151 Tumer syndrome RGO:23151 ICD10CM:K55.2 SNOMEDCT:197244008 RGO:23158 Angiodysplasia of colon RGO:23158 SNOMEDCT:109558001 RGO:23159 Dieulafoy disease RGO:23159 RGO:23161 familial bile duct dilatation RGO:23161 RADLEX:RID4595 SNOMEDCT:235669002 RGO:23165 efferent loop syndrome RGO:23165 DOID:9778 ICD10CM:K58 RADLEX:RID5251 SNOMEDCT:10743008 RGO:23167 irritable bowel syndrome RGO:23167 ORDO:1876 RGO:23168 oculogastrointestinal muscular dystrophy RGO:23168 DOID:3191 ICD10CM:G71.2 ORDO:607 SNOMEDCT:75072002 RGO:23170 nemaline myopathy RGO:23170 ORDO:99723 RGO:23171 familial esophageal atresia RGO:23171 RGO:23173 familial omphalocele RGO:23173 HP:0003196 RGO:23174 hypoplastic nose RGO:23174 RGO:23175 rudimentary auricles RGO:23175 RGO:23177 familial gastroschisis RGO:23177 SNOMEDCT:17322007 RGO:23179 parasitic infection RGO:23179 RGO:23181 rheumatic valvular disease RGO:23181 HP:0001642 SNOMEDCT:56786000 RGO:23183 pulmonic valve stenosis RGO:23183 RGO:23185 pulmonary artery rupture RGO:23185 DOID:0050306 ORDO:86 SNOMEDCT:715364001 RGO:23186 familial abdominal aortic aneurysm RGO:23186 RGO:23187 familial intracranial aneurysm RGO:23187 RGO:23189 medial agenesis RGO:23189 RGO:23191 Berry syndrome RGO:23191 RGO:23192 distal aortopulmonary window RGO:23192 RGO:23193 aortic origin of right pulmonary artery RGO:23193 RGO:23196 marfanoid hypermobility syndrome RGO:23196 RGO:23202 red-eyed shunt syndrome RGO:23202 RGO:23207 potassium-sensitive periodic paralysis RGO:23207 RGO:23208 ventricular ectopy RGO:23208 SNOMEDCT:253978002 RGO:23209 dysmorphic features RGO:23209 DOID:0050476 ICD10CM:E78.71 ORDO:111 SNOMEDCT:297231002 RGO:23218 Barth syndrome RGO:23218 DOID:0050461 SNOMEDCT:54954004 RGO:23219 aspartylglycosaminuria RGO:23219 DOID:9883 ORDO:98895 SNOMEDCT:387732009 RGO:23220 Becker muscular dystrophy RGO:23220 magnesium depletion RGO:23221 chronic magnesium deficiency RGO:23221 SPCD carnitine deficiency carnitine transporter deficiency carnitine uptake defect systemic carnitine deficiency systemic primary carnitine deficiency HP:0003234 RGO:23222 carnitine deficiency syndrome RGO:23222 RGO:23223 recurrent neutropenia RGO:23223 SNOMEDCT:35728003 RGO:23224 familial cardiomyopathy RGO:23224 DOID:11727 ICD10CM:G71.0 ORDO:269 SNOMEDCT:399091004 RGO:23226 facioscapulohumeral muscular dystrophy RGO:23226 RGO:23227 familial hypermethioninemia RGO:23227 DOID:0050083 ICD10CM:E59 SNOMEDCT:46939000 RGO:23229 Keshan disease RGO:23229 HP:0001324 RGO:23232 muscular weakness RGO:23232 DOID:8545 HP:0002047 ORDO:423 SNOMEDCT:405501007 RGO:23233 malignant hyperthermia RGO:23233 DOID:11724 HP:0006785 ICD10CM:G71.0 SNOMEDCT:93153005 RGO:23234 limb-girdle muscular dystrophy RGO:23234 ORDO:5 ORDO:99900 RGO:23235 long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency RGO:23235 RGO:23236 mannosidosis type 1 RGO:23236 DOID:0080013 SNOMEDCT:240096000 RGO:23237 mitochondrial disease RGO:23237 RGO:23240 Najjar syndrome RGO:23240 RGO:23244 linear skin defects RGO:23244 RGO:23245 polymyositis-dermatomyositis RGO:23245 DOID:3390 HP:0000972 RGO:23246 palmoplantar keratosis RGO:23246 ORDO:3115 RGO:23247 polyneuropathy of Roussy-Lévy RGO:23247 SNOMEDCT:25362006 RGO:23248 Refsum syndrome RGO:23248 DOID:8449 SNOMEDCT:47903000 RGO:23249 vitamin B deficiency RGO:23249 MVPS DOID:0050533 SNOMEDCT:8074002 RGO:23250 mitral valve prolapse syndrome RGO:23250 SNOMEDCT:30213001 RGO:23253 acquired lymphedema RGO:23253 RGO:23254 familial congenital pulmonary lymphangiectasis RGO:23254 RGO:23255 generalized lymphangiomatosis RGO:23255 RGO:23256 hereditary lymphedema syndromes RGO:23256 RGO:23257 lymphedema-hypoparathyroidism syndrome RGO:23257 RGO:23259 primary lymphatic dysplasia RGO:23259 RGO:23263 post shunt procedure RGO:23263 DVT deep vein thrombosis HP:0002625 SNOMEDCT:128053003 RGO:23264 deep venous thrombosis RGO:23264 VTE venous thromboembolism SNOMEDCT:429098002 RGO:23267 venous thromboembolic disease RGO:23267 HP:0025107 ORDO:1556 SNOMEDCT:254778000 RGO:23270 cutis marmorata telangiectatica congenita RGO:23270 SNOMEDCT:49465005 RGO:23271 essential telangiectasia RGO:23271 RGO:23272 hereditary acrolabial telangiectasia RGO:23272 SNOMEDCT:238764001 RGO:23273 hereditary benign telangiectasia RGO:23273 RGO:23274 radiation-induced telangiectasia RGO:23274 RGO:23276 xeroderma pigmentosa RGO:23276 SNOMEDCT:2499000100000410 RGO:23278 mastoid fracture RGO:23278 RGO:23279 frontal sinus fracture RGO:23279 SNOMEDCT:263148008 RGO:23280 sphenoid sinus fracture RGO:23280 DOID:3842 RGO:23282 skull base neoplasm RGO:23282 DOID:3526 RGO:23283 cerebral infarct RGO:23283 DOID:11612 HP:0000147 SNOMEDCT:69878008 RGO:23288 polycystic ovaries RGO:23288 RGO:23289 pigmental retardation RGO:23289 HP:0000612 ICD10CM:Q13.0 ORDO:98944 SNOMEDCT:9446007 RGO:23290 coloboma of iris RGO:23290 RGO:23292 Boucher-Neuhäuser syndrome RGO:23292 HP:0001135 RGO:23294 chorioretinal dystrophy RGO:23294 SNOMEDCT:129609000 RGO:23295 spinocerebellar ataxia RGO:23295 SNOMEDCT:82725007 RGO:23296 fibrodysplasia ossificans congenita RGO:23296 RGO:23298 Jaffe-Campanacci syndrome RGO:23298 RGO:23299 Martsolf syndrome RGO:23299 DOID:14449 HP:0000133 ORDO:1772 SNOMEDCT:83579008 RGO:23300 mixed gonadal dysgenesis RGO:23300 RGO:23301 odontotrichomelic dysplasia RGO:23301 ORDO:3210 SNOMEDCT:403767009 RGO:23302 Summitt syndrome RGO:23302 DOID:2121 HP:0000968 SNOMEDCT:8654005 RGO:23303 ectodermal dysplasia RGO:23303 RGO:23307 ACTH therapy RGO:23307 RGO:23309 valproate therapy RGO:23309 HP:0100607 SNOMEDCT:266599000 RGO:23310 dysmenorrhea RGO:23310 DOID:11613 SNOMEDCT:237793004 RGO:23311 hyperandrogenism RGO:23311 RGO:23312 adrenal enzyme deficiency RGO:23312 RGO:23313 Shapiro syndrome RGO:23313 RGO:23314 maternal adrenocortical adenoma RGO:23314 ORDO:755 RGO:23315 Leydig cell hypoplasia RGO:23315 SNOMEDCT:425708006 RGO:23316 placental aromatase deficiency RGO:23316 SNOMEDCT:16424000 RGO:23317 glucagonoma syndrome RGO:23317 HP:0003097 RGO:23319 femoral hypoplasia RGO:23319 HP:0000995 RGO:23321 pigmented nevi RGO:23321 RGO:23322 chronic infection of globe RGO:23322 HP:0001382 RGO:23323 joint hyperextensibility RGO:23323 HP:0000558 ORDO:91483 RGO:23324 Rieger anomaly RGO:23324 HP:0000831 RGO:23326 insulin-resistant diabetes mellitus RGO:23326 DOID:12700 HP:0000870 ICD10CM:E22.1 SNOMEDCT:237662005 RGO:23327 hyperprolactinemia RGO:23327 RGO:23328 Stratton-Parker syndrome RGO:23328 RGO:23329 brachycamptodactly RGO:23329 ORDO:276399 RGO:23332 familial multinodular goiter RGO:23332 DOID:0060744 ORDO:705 SNOMEDCT:70348004 RGO:23333 Pendred syndrome RGO:23333 DOID:348 HP:0010749 ICD10CM:H02.3 SNOMEDCT:47704002 RGO:23334 blepharochalasis RGO:23334 SNOMEDCT:699762000 RGO:23335 double lip RGO:23335 ORDO:562 SNOMEDCT:36517007 RGO:23336 McCune-Albright syndrome RGO:23336 SNOMEDCT:699298009 RGO:23337 Young-Simpson syndrome RGO:23337 DOID:1673 HP:0002107 RADLEX:RID5352 SNOMEDCT:36118008 RGO:23339 pneumothorax RGO:23339 mediastinal emphysema HP:0025421 RADLEX:RID28523 SNOMEDCT:16838000 RGO:23340 pneumomediastinum RGO:23340 SNOMEDCT:233642001 RGO:23342 catamenial pneumothorax RGO:23342 RGO:23344 cytotoxic chemotherapy RGO:23344 RGO:23345 postoperative bronchopleural fistula RGO:23345 RGO:23346 suppurative pneumonia RGO:23346 RGO:23349 interstitial pulmonary fibrosis RGO:23349 RGO:23351 familial fibrocystic dysplasia RGO:23351 RGO:23352 pulmonary interstitial emphysema RGO:23352 DOID:11049 ICD10CM:P24.0 ORDO:70588 RGO:23353 meconium aspiration RGO:23353 RGO:23354 pneumothorax of newborn RGO:23354 RGO:23355 ruptured pulmonary hydatid cyst RGO:23355 RGO:23356 ruptured amebic abscess RGO:23356 Shaver disease SNOMEDCT:14700006 RGO:23357 bauxite pneumoconiosis RGO:23357 RGO:23359 intrauterine anuria RGO:23359 RGO:23360 blunt chest injury RGO:23360 RGO:23361 tracheobronchial injury RGO:23361 RGO:23362 penetrating chest injury RGO:23362 DOID:2158 RGO:23363 lung metastasis RGO:23363 RGO:23365 carcinoma of adrenals RGO:23365 ICD10CM:J93.11 SNOMEDCT:328561000119107 RGO:23366 primary spontaneous pneumothorax RGO:23366 SNOMEDCT:177765008 RGO:23369 thoracotomy RGO:23369 SNOMEDCT:48387007 RGO:23371 tracheotomy RGO:23371 RGO:23373 percutaneous biopsy RGO:23373 RGO:23374 transbronchial biopsy RGO:23374 RGO:23375 subclavian puncture RGO:23375 SNOMEDCT:233527006 RGO:23376 central line insertion RGO:23376 RGO:23377 overinflation of positive pressure ventilation RGO:23377 RADLEX:RID49475 RGO:23378 pacemaker insertion RGO:23378 RGO:23379 pneumatocele rupture RGO:23379 RGO:23380 pulmonary cyst rupture RGO:23380 RGO:23381 idiopathic isolated congenital tracheobronchial calcification RGO:23381 RGO:23382 warfarin therapy RGO:23382 RGO:23383 dentate nucleus calcification RGO:23383 HP:0006960 RGO:23384 choroid plexus calcification RGO:23384 RGO:23385 dural calcification RGO:23385 RGO:23386 Intracranial infection RGO:23386 RGO:23387 low-grade astrocytoma RGO:23387 RGO:23388 congenital cerebral granuloma RGO:23388 RGO:23389 chronic intracerebral hematoma RGO:23389 RGO:23391 interclinoid ligament calcification RGO:23391 RGO:23392 osteosarcoma metastasis RGO:23392 RGO:23394 pineal germinoma RGO:23394 RGO:23396 tubercular meningitis RGO:23396 RGO:23397 habenular commissure calcification RGO:23397 RGO:23398 pacchionian granulation calcification RGO:23398 RGO:23399 petroclinoid ligament calcification RGO:23399 HP:0012682 RGO:23400 pineal gland calcification RGO:23400 HP:0100699 RADLEX:RID3829 SNOMEDCT:48677004 RGO:23401 scarring RGO:23401 RGO:23402 opportunistic infections RGO:23402 DOID:646 SNOMEDCT:34476008 RGO:23404 viral encephalitis RGO:23404 ICD10CM:P35.1 SNOMEDCT:59527008 RGO:23406 congenital cytomegalovirus infection RGO:23406 RGO:23407 congenital measles RGO:23407 RGO:23408 congenital chickenpox RGO:23408 RGO:23409 congenital poliomyelitis RGO:23409 RGO:23414 chronic epidural hematoma RGO:23414 persistent infantile bladder RADLEX:RID5300 SNOMEDCT:404220000 RGO:23415 bladder instability RGO:23415 RGO:23418 aniridia-Wilms tumor RGO:23418 ORDO:96176 RGO:23420 ring chromosome 13 RGO:23420 RGO:23421 chromosome 13q- syndrome RGO:23421 ORDO:753 RGO:23422 5-alpha-reductase deficiency RGO:23422 HP:0010458 SNOMEDCT:8800006 RGO:23423 female pseudohermaphroditism RGO:23423 HP:0010459 SNOMEDCT:18978002 RGO:23424 true hermaphroditism RGO:23424 RGO:23429 idiopathic scrotal calcification RGO:23429 RGO:23430 meconium periorchitis RGO:23430 RADLEX:RID1801 SNOMEDCT:85419002 RGO:23431 orchiopexy RGO:23431 DOID:5104 SNOMEDCT:33793000 RGO:23432 testicular infarction RGO:23432 RGO:23433 pulmonary microlithiasis RGO:23433 DOID:0060350 ORDO:976 RGO:23434 adenine phosphoribosyltransferase deficiency RGO:23434 RGO:23435 corticosteroid excess RGO:23435 SNOMEDCT:37497004 RGO:23436 enteric hyperoxaluria RGO:23436 ORDO:94088 RGO:23437 hereditary renal hypouricemia RGO:23437 ICD10CM:E53.1 SNOMEDCT:386080007 RGO:23438 pyridoxine deficiency RGO:23438 RGO:23440 chronic nephritis RGO:23440 ORDO:336 RGO:23441 fibromuscular arterial dysplasia RGO:23441 SNOMEDCT:35787005 RGO:23444 postinflammatory atrophy RGO:23444 RGO:23446 vincristine administration RGO:23446 DOID:14753 ICD10CM:E71.110 ORDO:33 SNOMEDCT:87827003 RGO:23449 isovaleric acidemia RGO:23449 DOID:14749 HP:0002912 ICD10CM:E71.120 SNOMEDCT:42393006 RGO:23450 methylmalonic acidemia RGO:23450 RGO:23451 muscular cytochrome c oxidase deficiency RGO:23451 3-hydroxy-3-methylglutaryl-CoA lyase deficiency HMG-CoA lyase deficiency hydroxymethylglutaric aciduria RGO:23452 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency RGO:23452 SNOMEDCT:428752002 RGO:23454 recent myocardial infarction RGO:23454 RGO:23455 recent cardiac surgery RGO:23455 HP:0003048 RGO:23457 radial head subluxation RGO:23457 RGO:23461 inflammation of orbital apex RGO:23461 patellar aplasia HP:0006443 SNOMEDCT:309244002 RGO:23462 absent patella RGO:23462 RGO:23463 hypoplastic patella RGO:23463 RGO:23464 calcific flecks in patella RGO:23464 HP:0001571 ICD10CM:K01.1 SNOMEDCT:235104008 RGO:23465 impacted teeth RGO:23465 RGO:23467 cervical segmentation malformation RGO:23467 RGO:23469 painful adipositis RGO:23469 SNOMEDCT:64383006 RGO:23470 infantile spinal muscular atrophy RGO:23470 RGO:23473 brain stem atrophy RGO:23473 SNOMEDCT:263029007 RGO:23474 dislocated patella RGO:23474 RGO:23476 adrenocortical tumor RGO:23476 DOID:4966 SNOMEDCT:237777008 RGO:23477 adrenocortical hyperplasia RGO:23477 RGO:23478 elbow joint subluxation RGO:23478 HP:0002937 RGO:23480 hemivertebrae RGO:23480 HP:0000691 ICD10CM:K00.2 SNOMEDCT:32337007 RGO:23481 microdontia RGO:23481 RGO:23482 small antimongoloid pelvis with vertical ilia RGO:23482 RGO:23483 steep acetabular angle RGO:23483 RGO:23485 low acetabular angle RGO:23485 HP:0003414 ORDO:99666 SNOMEDCT:45179004 RGO:23486 atlantoaxial subluxation RGO:23486 RGO:23487 hypoplastic, flared iliac wings RGO:23487 RGO:23488 decreased acetabular angle RGO:23488 RGO:23489 decreased iliac angle RGO:23489 RGO:23490 ischial tapering RGO:23490 RGO:23491 orbital hypotelorism with arrhinencephaly RGO:23491 RGO:23495 vaginal foreign body RGO:23495 SNOMEDCT:70176004 RGO:23496 rectal foreign body RGO:23496 RGO:23497 bladder rhabdomyosarcoma RGO:23497 ORDO:206492 RGO:23498 vaginal rhabdomyosarcoma RGO:23498 RGO:23499 bone lesion RGO:23499 RGO:23500 enterolith in Meckel diverticulum RGO:23500 RGO:23501 enterolith in colonic diverticulum RGO:23501 RGO:23502 ligament calcification RGO:23502 RGO:23503 appendiceal myxoglobulosis RGO:23503 RGO:23506 colloid carcinoma of appendix RGO:23506 HP:0000897 SNOMEDCT:15214001 RGO:23507 rachitic rosary RGO:23507 RGO:23508 healed fracture with callus RGO:23508 RGO:23509 healed osteomyelitis RGO:23509 RGO:23512 ventriculography needle tracks RGO:23512 RGO:23513 habenula calcification RGO:23513 DOID:9795 ICD10CM:A17.0 SNOMEDCT:58437007 RGO:23514 tuberculous meningitis RGO:23514 RGO:23515 healed brain abscess RGO:23515 RGO:23516 familial idiopathic basal ganglia calcification RGO:23516 RGO:23518 congenital rubella RGO:23518 RGO:23519 coxsackie B RGO:23519 RGO:23521 giant aneurysm RGO:23521 RGO:23522 acute intracerebral hemorrhage RGO:23522 RGO:23525 acute epidural hemorrhage RGO:23525 RGO:23526 acute subdural hemorrhage RGO:23526 RGO:23527 hemorrhagic metastasis RGO:23527 RGO:23529 adenocarcinoma colon RGO:23529 RGO:23530 subacute subdural hematoma RGO:23530 RGO:23532 intracerebral abscess RGO:23532 DOID:6811 RGO:23533 juvenile pilocytic astrocytoma RGO:23533 RGO:23534 resolving intracerebrall hematoma RGO:23534 RGO:23535 resolving subdural hematoma RGO:23535 RGO:23536 globus pallidus necrosis RGO:23536 PML DOID:643 ICD10CM:A81.2 ORDO:217260 SNOMEDCT:22255007 RGO:23537 progressive multifocal leukoencephalopathy RGO:23537 RGO:23539 pineal teratocarcinoma RGO:23539 ORDO:984 SNOMEDCT:66489009 RGO:23540 pulmonary agenesis RGO:23540 RGO:23541 rotated patient RGO:23541 moyamoya disease moyamoya syndrome multiple progressive intracranial artery occlusions with telangiectasia RGO:23550 moyamoya RGO:23550 ORDO:838 SNOMEDCT:702575003 RGO:23551 Susac syndrome RGO:23551 ORDO:3243 SNOMEDCT:84625002 RGO:23552 Sweet syndrome RGO:23552 RGO:23554 mucopolysaccharidosis 1-H/S RGO:23554 ICD10CM:Q87.0 RGO:23555 Robin syndrome RGO:23555 RGO:23556 Avasthey-Roy syndrome RGO:23556 RGO:23558 platelet storage pool disease RGO:23558 SNOMEDCT:257549005 RGO:23560 chemical injury RGO:23560 HP:0002960 SNOMEDCT:85828009 RGO:23561 autoimmune disorder RGO:23561 DOID:9080 SNOMEDCT:190817009 RGO:23562 macroglobulinemia RGO:23562 RGO:23563 tumor-produced globulins RGO:23563 RGO:23564 mechanical constriction RGO:23564 SNOMEDCT:63995005 RGO:23565 bandage RGO:23565 RGO:23566 baby mittens RGO:23566 RGO:23567 hair band RGO:23567 SNOMEDCT:392247006 RGO:23568 arterial catheterization RGO:23568 RGO:23570 ring contraction RGO:23570 RGO:23571 annular band RGO:23571 HP:0003634 RGO:23572 amyoplasia RGO:23572 RGO:23573 bacterial abscess RGO:23573 DOID:3763 SNOMEDCT:237821001 RGO:23576 hermaphroditism RGO:23576 RGO:23577 complete vaginal atresia RGO:23577 RGO:23578 distal urogenital sinus RGO:23578 HP:0001153 RGO:23579 double vagina RGO:23579 RGO:23580 labial fusion RGO:23580 ORDO:1092 RGO:23581 renal-genital-middle ear syndrome RGO:23581 RGO:23582 uterovaginal hypoplasia RGO:23582 RGO:23584 pelvic irradiation RGO:23584 RGO:23585 renal-genital-ear anomaly syndrome RGO:23585 ORDO:91500 RGO:23586 acute interstitial nephritis and uveitis syndrome RGO:23586 amelogenesis imperfecta and nephrocalcinosis syndrome ORDO:1031 RGO:23587 amelogenesis imperfecta - nephrocalcinosis RGO:23587 RGO:23588 Hutterite cerebro-osteonephrodysplasia RGO:23588 RGO:23589 spondylorhizomelic dwarfism RGO:23589 Wolcott-Rallison dysplasia DOID:0090060 ORDO:1667 SNOMEDCT:254066006 RGO:23590 Wolcott-Rallison syndrome RGO:23590 DOID:12251 HP:0004319 ICD10CM:E27.40 SNOMEDCT:60086000 RGO:23592 hypoaldosteronism RGO:23592 SNOMEDCT:30178006 RGO:23596 vitamin D RGO:23596 SNOMEDCT:233778002 RGO:23598 tracheal fistula RGO:23598 HP:0002617 RADLEX:RID4743 SNOMEDCT:25322007 RGO:23600 dilatation RGO:23600 SNOMEDCT:3830001 RGO:23601 subcutaneous emphysema RGO:23601 RGO:23602 facial fracture RGO:23602 SNOMEDCT:178283002 RGO:23603 neck dissection RGO:23603 RGO:23604 infection with gas-forming organism RGO:23604 SNOMEDCT:27779004 RGO:23605 sternotomy RGO:23605 RADLEX:RID1600 SNOMEDCT:45900003 RGO:23606 esophagectomy RGO:23606 RGO:23608 gas insufflation RGO:23608 RGO:23609 rupture of trachea RGO:23609 SNOMEDCT:262786004 RGO:23610 rupture of bronchus RGO:23610 RGO:23613 spontaneous pneumomediastinum RGO:23613 DOID:14702 RGO:23616 branchiootorenal syndrome RGO:23616 Cumming dysplasia ORDO:1318 RGO:23619 Cumming syndrome RGO:23619 RGO:23620 polycystic hepatic dysplasia RGO:23620 RGO:23621 polycystic pancreatic dysplasia RGO:23621 ORDO:2111 SNOMEDCT:707530009 RGO:23622 cystic hamartoma of lung and kidney RGO:23622 DOID:0060358 RGO:23624 glutaric aciduria type 2 RGO:23624 RGO:23625 obstructive cystic disease RGO:23625 RGO:23628 posttraumatic pseudocyst RGO:23628 RGO:23629 segmental cystic dysplasia RGO:23629 RGO:23633 traumatic arteriovenous fistula of azygos vein RGO:23633 RGO:23634 bulging interlobar fissure RGO:23634 RGO:23637 atresia of thoracic duct RGO:23637 SNOMEDCT:91293009 RGO:23638 congenital lymphangiectasia RGO:23638 RGO:23640 surgical injury to thoracic duct RGO:23640 RGO:23641 surgery for congenital heart disease RGO:23641 HP:0004933 RGO:23642 ascending aortic dissection RGO:23642 SNOMEDCT:386041004 RGO:23645 perihepatitis RGO:23645 SNOMEDCT:237041005 RGO:23646 Fitz-Hugh-Curtis syndrome RGO:23646 RGO:23647 perforated cholecystitis RGO:23647 RGO:23648 perforated hepatic abscess RGO:23648 SNOMEDCT:255121007 RGO:23649 peritoneal carcinomatosis RGO:23649 RGO:23650 inflammation of peritoneal capsule of liver RGO:23650 RGO:23651 hepatic capsular enhancement RGO:23651 RGO:23652 enhancement of liver capsule RGO:23652 RGO:23654 pulmonic valvular atresia RGO:23654 RGO:23657 resolving hemorrhage RGO:23657 RGO:23658 low grade astrocytoma RGO:23658 RGO:23659 cerebral gliomatosis RGO:23659 RGO:23660 contusions RGO:23660 RGO:23661 neurotrichinosis RGO:23661 RGO:23662 grade II astrocytoma RGO:23662 SNOMEDCT:13691000119103 RGO:23663 epidural empyema RGO:23663 RGO:23664 resolving intracerebral hematoma RGO:23664 RGO:23665 resolving infarction RGO:23665 DOID:6544 RADLEX:RID4112 SNOMEDCT:128914005 RGO:23666 atypical meningioma RGO:23666 RGO:23667 cholesterol cyst RGO:23667 RGO:23668 late subacute hematoma RGO:23668 SNOMEDCT:58190003 RGO:23669 blood flow RGO:23669 RADLEX:RID14116 RGO:23670 posterior pituitary RGO:23670 SNOMEDCT:193078005 RGO:23676 pseudomeningocele RGO:23676 SNOMEDCT:8573003 RGO:23677 acute hemorrhage RGO:23677 RGO:23678 complex arachnoid cyst RGO:23678 RGO:23683 hyperacute hemorrhage RGO:23683 RGO:23684 acute subarachnoid hemorrhage RGO:23684 ORDO:247245 RADLEX:RID5211 RGO:23685 superficial siderosis RGO:23685 RGO:23686 idiopathic patella alta RGO:23686 RGO:23687 chronic subluxation RGO:23687 RGO:23688 idiopathic bowlegs RGO:23688 RGO:23689 prenatal bowing RGO:23689 RGO:23690 subchondral cyst RGO:23690 DOID:2557 ICD10CM:M94.2 RADLEX:RID5400 SNOMEDCT:63198006 RGO:23691 chondromalacia RGO:23691 RGO:23693 Schmid type RGO:23693 RGO:23696 sacral hypoplasia RGO:23696 RGO:23698 chronic muscular hypotonia RGO:23698 happy puppet syndrome DOID:1932 ICD10CM:Q93.5 ORDO:72 SNOMEDCT:76880004 RGO:23699 Angelman syndrome RGO:23699 RGO:23700 perinatal brain hypoxia RGO:23700 RGO:23701 chromosome 7:del(7q) syndrome RGO:23701 RGO:23702 chromosome 9:dup (9p) syndrome RGO:23702 chromosome 18q- syndrome RGO:23703 chromosome 18:del(18q) syndrome RGO:23703 universal craniosynostosis RGO:23704 total craniosynostosis RGO:23704 idiopathic small brain SNOMEDCT:1829003 RGO:23706 micrencephaly RGO:23706 SNOMEDCT:95850008 RGO:23708 depressed skull fracture RGO:23708 RADLEX:RID35201 RGO:23709 fat halo sign RGO:23709 RGO:23710 submucosal colonic fat deposition RGO:23710 RGO:23711 cytoreductive therapy RGO:23711 SNOMEDCT:267388009 RGO:23713 idiopathic hypopituitarism RGO:23713 HP:0010585 RGO:23714 small epiphyses RGO:23714 HP:0002866 RGO:23717 small iliac wings RGO:23717 RGO:23719 poor dentin RGO:23719 HP:0006336 RGO:23720 short dental roots RGO:23720 RGO:23721 opalescent teeth RGO:23721 RGO:23724 gonadal tumor RGO:23724 RGO:23725 coxa magna and plana RGO:23725 RGO:23726 healed Legg-Perthes disease RGO:23726 RGO:23727 Perthes-like femoral heads RGO:23727 RGO:23728 chronic infectious arthritis RGO:23728 ORIF SNOMEDCT:133863002 RGO:23729 open reduction with internal fixation RGO:23729 RGO:23731 localized hyperemia RGO:23731 SNOMEDCT:70737009 RGO:23733 Hunter disease RGO:23733 RGO:23734 vitamin D-deficient rickets type B RGO:23734 ORDO:100978 RGO:23735 cloverleaf skull deformity with thanatophoric dysplasia RGO:23735 RGO:23736 restricted movement during growth RGO:23736 HP:0002982 RGO:23737 tibial bowing RGO:23737 RGO:23738 physiologic bowlegs RGO:23738 RGO:23744 surgically regenerated rib RGO:23744 ICD10CM:E34.4 SNOMEDCT:237835004 RGO:23745 constitutional tall stature RGO:23745 RGO:23749 primary pinealoma RGO:23749 RGO:23750 acquired hyperthyroidism RGO:23750 RGO:23751 ectopic gonadotropin production RGO:23751 RGO:23753 congenital dwarfism RGO:23753 RGO:23754 congenital mental retardation RGO:23754 RGO:23755 idiopathic delayed growth RGO:23755 SNOMEDCT:432526008 RGO:23756 familial short stature RGO:23756 RGO:23757 severe constitutional disease RGO:23757 RGO:23758 chronic illness RGO:23758 RGO:23759 hypopituitarism with growth hormone deficiency RGO:23759 DOID:0050470 ORDO:508 SNOMEDCT:111307005 RGO:23761 leprechaunism RGO:23761 RGO:23763 idiopathic pseudofracture RGO:23763 RGO:23764 neuropathic disorder RGO:23764 RGO:23765 bone graft donor site RGO:23765 SNOMEDCT:32322008 RGO:23766 subchondral bone cyst RGO:23766 RGO:23767 vacuum cyst RGO:23767 RGO:23768 pneumatocyst RGO:23768 RADLEX:RID5363 RGO:23769 fracture nonunion RGO:23769 RGO:23772 major joint replacement RGO:23772 RGO:23773 posttraumatic degenerative arthritis RGO:23773 RGO:23775 lymphoma after radiation therapy RGO:23775 RGO:23776 calcifying metastasis RGO:23776 RGO:23777 perilabral cyst RGO:23777 RADLEX:RID11812 SNOMEDCT:3829006 RGO:23778 iron RGO:23778 RGO:23783 carotid siphon aneurysm RGO:23783 HP:0011755 RGO:23784 ectopic posterior pituitary RGO:23784 RGO:23785 optic chiasm glioma RGO:23785 SNOMEDCT:237714006 RGO:23786 tuber cinereum hamartoma RGO:23786 RGO:23787 mandibular schwannoma RGO:23787 RGO:23788 pituitary hyperplasia RGO:23788 RGO:23789 pituitary choristoma RGO:23789 RGO:23790 pituitary adenocarcinoma RGO:23790 RGO:23791 pituitary carcinosarcoma RGO:23791 RGO:23792 pituitary lymphoma RGO:23792 RGO:23793 pituitary oncocytoma RGO:23793 RGO:23794 sphenoid sinus mucocele RGO:23794 RGO:23795 sphenoid sinus carcinoma RGO:23795 ORDO:95512 RGO:23798 adenohypophysitis RGO:23798 HP:0410049 RGO:23799 isolated radial ray anomaly RGO:23799 RGO:23800 ulnofibular dysplasia RGO:23800 Reinhardt-Pfeiffer dysplasia ORDO:2634 RGO:23801 mesomelic dysplasia Reinhardt-Pfeiffer type RGO:23801 RGO:23802 mesomelic dysplasia Werner type RGO:23802 RGO:23804 isolated forearm deformity RGO:23804 RGO:23805 generalized bone growth disturbance RGO:23805 RGO:23806 underconstriction of diametaphyses RGO:23806 RGO:23807 overconstriction of diametaphyses RGO:23807 RGO:23808 isolated elbow anomaly RGO:23808 SNOMEDCT:363162000 RGO:23809 joint infection RGO:23809 RGO:23811 isolated scapula anomaly RGO:23811 PLSD RGO:23812 platyspondylic lethal skeletal dysplasia RGO:23812 RGO:23814 chronic productive osteomyelitis RGO:23814 RGO:23815 cartilaginous tumor RGO:23815 SNOMEDCT:234012008 RGO:23816 traumatic arteriovenous fistula RGO:23816 RGO:23817 Hill-Sachs defect RGO:23817 RGO:23818 chronic dislocation RGO:23818 RGO:23819 neuroarthropathy RGO:23819 SNOMEDCT:237716008 RGO:23820 pituitary cyst RGO:23820 RGO:23821 sphenoid sinus neoplasm RGO:23821 RGO:23822 internal carotid artery aneurysm RGO:23822 RGO:23823 internal carotid artery ectasia RGO:23823 RADLEX:RID5237 SNOMEDCT:698081007 RGO:23824 perineural spread RGO:23824 DOID:3575 RGO:23825 cavernous sinus thrombosis RGO:23825 SNOMEDCT:80595007 RGO:23827 glomus jugulare RGO:23827 RGO:23828 glomus vagale RGO:23828 RGO:23829 temporal lobe glioma RGO:23829 RGO:23830 temporal lobe hematoma RGO:23830 RGO:23831 temporal lobe abscess RGO:23831 RGO:23832 paranasal sinus malignancy RGO:23832 SNOMEDCT:89511000119106 RGO:23833 subdural hygroma RGO:23833 RGO:23835 treated Hodgkin disease RGO:23835 RGO:23838 mucinous breast adenocarcinoma RGO:23838 RGO:23841 papillary thyroid adenocarcinoma RGO:23841 RGO:23842 papillary ovarian adenocarcinoma RGO:23842 RGO:23843 dystrophic metastatic calcification RGO:23843 RGO:23845 diffuse atherosclerosis RGO:23845 SNOMEDCT:195911009 RGO:23846 chickenpox pneumonia RGO:23846 RGO:23847 smallpox handler lung RGO:23847 RGO:23848 multiple hamartomas of lung RGO:23848 RGO:23849 pulmonary artery atherosclerosis RGO:23849 SNOMEDCT:204311009 RGO:23850 Eisenmenger complex RGO:23850 RGO:23851 old empyema RGO:23851 RGO:23853 healed rib fractures RGO:23853 HP:0100760 SNOMEDCT:53148007 RGO:23855 clubbing of toes RGO:23855 macrodactyly simplex congenita RGO:23856 idiopathic macrodactyly RGO:23856 RGO:23858 congenital acro-osteolysis RGO:23858 RGO:23859 congenital short metacarpals RGO:23859 RGO:23860 congenital short metatarsals RGO:23860 RGO:23861 epiphyseal cartilage injury RGO:23861 RGO:23862 idiopathic brachydactyly RGO:23862 RGO:23863 congenital short phalanges RGO:23863 RGO:23866 congenital block vertebrae RGO:23866 RGO:23867 tuberculosis spondylitis RGO:23867 RGO:23868 ovoid thoracic vertebral body RGO:23868 RGO:23869 ovoid lumbar vertebral body RGO:23869 RGO:23870 Smith-Lemli-Opitz syndrome type 2 RGO:23870 RGO:23871 convulsions RGO:23871 HP:0001281 ICD10CM:R29.0 SNOMEDCT:10629009 RGO:23873 tetany RGO:23873 SNOMEDCT:3723001 RGO:23877 inflammatory arthritis RGO:23877 RGO:23878 seronegative psoriatic arthritis RGO:23878 RGO:23880 sclerotic hand bone lesion RGO:23880 RGO:23881 sclerotic foot bone lesion RGO:23881 RGO:23883 carcinoma of nail-bed RGO:23883 DOID:3451 RGO:23884 carcinoma of skin RGO:23884 RGO:23885 palm thorn RGO:23885 SNOMEDCT:239792003 RGO:23886 seronegative rheumatoid arthritis RGO:23886 RGO:23887 adult rheumatoid arthritis RGO:23887 RGO:23891 small-cell osteosarcoma RGO:23891 DOID:6489 RADLEX:RID4022 SNOMEDCT:128772005 RGO:23892 periosteal osteosarcoma RGO:23892 RGO:23894 mesenchymal osteosarcoma RGO:23894 healed fractures RGO:23897 healed fracture RGO:23897 RGO:23900 renal capsular osteosarcoma RGO:23900 RGO:23901 soft-tissue osteosarcoma RGO:23901 atlantooccipital fusion occipitalization of atlas SNOMEDCT:178547005 RGO:23906 atlanto-occipital fusion RGO:23906 RGO:23907 hypoplasia of occipital condyle RGO:23907 SNOMEDCT:16496009 RGO:23908 atlantoaxial fusion RGO:23908 RGO:23909 atlantoaxial malsegmentation RGO:23909 tertiary condyle RGO:23910 third occipital condyle RGO:23910 RGO:23912 odontoid dysplasia with atlantoaxial dislocation RGO:23912 separate odontoid HP:0005667 SNOMEDCT:445242006 RGO:23913 os odontoideum RGO:23913 RGO:23916 hypoplasia of dens RGO:23916 RGO:23917 aplasia of dens RGO:23917 RGO:23918 craniovertebral junction abnormality RGO:23918 RGO:23919 degenerative lesion RGO:23919 RGO:23920 primary skull base neoplasm RGO:23920 RGO:23921 metastasis to skull base RGO:23921 DOID:10437 RGO:23923 metastasis to lymph node RGO:23923 lymphangiosarcoma due to chronic lymphedema SNOMEDCT:62497000 RGO:23924 Stewart-Treves syndrome RGO:23924 SNOMEDCT:443524000 RGO:23926 secondary osteoarthritis RGO:23926 RGO:23928 excess mechanical stress RGO:23928 RADLEX:RID39218 SNOMEDCT:417893002 SNOMEDCT:6081001 RGO:23929 deformity RGO:23929 RADLEX:RID4766 SNOMEDCT:399898009 RGO:23930 malalignment RGO:23930 RGO:23931 cartilage hypertrophy RGO:23931 SNOMEDCT:22200009 RGO:23932 bone resorption RGO:23932 RGO:23933 neuropathic arthropathy hypertrophic type RGO:23933 RGO:23934 ligamentum teres rupture RGO:23934 RGO:23935 retained cartilage fragment RGO:23935 RGO:23936 developmental joint dysplasia RGO:23936 RGO:23937 metastatic bone neoplasm RGO:23937 SNOMEDCT:24734008 SNOMEDCT:276433004 RGO:23938 insect bite RGO:23938 RGO:23939 nodular sclerosing Hodgkin disease RGO:23939 RGO:23941 intrathoracic adenomatous goiter RGO:23941 thymic lesion thymus mass RGO:23942 thymic mass RGO:23942 SNOMEDCT:21181001 RGO:23944 benign thymoma RGO:23944 RGO:23947 perforated central venous catheter RGO:23947 RGO:23948 loculated paramediastinal pleural effusion RGO:23948 RGO:23949 ascites extending through esophageal hiatus RGO:23949 RGO:23950 dilated fluid-filled esophagus RGO:23950 HP:0100751 RGO:23952 esophageal tumor RGO:23952 SNOMEDCT:197127002 RGO:23953 post-vagotomy syndrome RGO:23953 RGO:23954 hypodense brainstem lesion RGO:23954 T1-dark brainstem lesion RGO:23955 T1-hypointense brainstem lesion RGO:23955 RGO:23956 acute cortical infarction RGO:23956 RGO:23957 subacute cortical infarction RGO:23957 RGO:23958 late subacute cortical infarction RGO:23958 RGO:23959 chronic cortical infarction RGO:23959 RGO:23960 dural neoplasm RGO:23960 DOID:4956 RGO:23961 leptomeningeal neoplasm RGO:23961 RGO:23962 cortical arteriovenous malformation RGO:23962 dural AVM SNOMEDCT:84873005 RGO:23963 dural arteriovenous malformation RGO:23963 RGO:23964 subacute subarachnoid hemorrhage RGO:23964 RGO:23965 chronic subarachnoid hemorrhage RGO:23965 DOID:4794 HP:0030066 ORDO:251880 RADLEX:RID4406 SNOMEDCT:21589007 SNOMEDCT:715901002 RGO:23966 ependymoblastoma RGO:23966 RGO:23967 vertebral artery ectasia RGO:23967 SNOMEDCT:297176007 RGO:23968 vertebral artery aneurysm RGO:23968 RGO:23969 basilar artery ectasia RGO:23969 RGO:23970 basilar artery aneurysm RGO:23970 SNOMEDCT:713861002 RGO:23973 subdural effusion RGO:23973 RGO:23974 hypertrophic pachymeningitis RGO:23974 cavum septum pellucidum fifth ventricle RADLEX:RID6527 SNOMEDCT:369196003 SNOMEDCT:74968005 RGO:23975 cavum septi pellucidi RGO:23975 sixth ventricle SNOMEDCT:33191008 RGO:23979 cavum vergae RGO:23979 RGO:23984 subependymal nodule RGO:23984 RGO:23985 cervical-occipital encephalocele RGO:23985 RGO:23986 cervical-occipital meningocele RGO:23986 RGO:23987 upper cervical spine neoplasm RGO:23987 SNOMEDCT:301061006 RGO:23988 stenosis of external auditory canal RGO:23988 ORDO:141074 SNOMEDCT:26061003 RGO:23992 absence of external auditory canal RGO:23992 RGO:23994 chondroid tumor RGO:23994 SNOMEDCT:115239009 RGO:23995 bone tumor RGO:23995 RGO:23996 bony EAC stenosis RGO:23996 RGO:23997 membranous EAC stenosis RGO:23997 benign ceruminous adenoma DOID:7549 HP:0040097 RGO:23999 ceruminoma RGO:23999 RGO:24001 invasive keratitis RGO:24001 RGO:24002 cancellous osteoma RGO:24002 RGO:24004 retrofenestral otosclerosis RGO:24004 ICD10CM:H80.2 SNOMEDCT:91108004 RGO:24005 cochlear otosclerosis RGO:24005 HP:0030064 SNOMEDCT:128858006 RGO:24008 neurocytoma RGO:24008 RGO:24009 trapped ventricle RGO:24009 RGO:24011 ependymal adhesion RGO:24011 SNOMEDCT:71981002 RGO:24012 ependymitis RGO:24012 RGO:24013 infiltrating corpus callosum neoplasm RGO:24013 RGO:24014 septum pellucidum neoplasm RGO:24014 RGO:24015 septum pellucidum cyst RGO:24015 RGO:24016 intraventricular astrocytoma RGO:24016 DOID:6294 RGO:24017 corpus callosum lipoma RGO:24017 RGO:24018 third ventricle neoplasm RGO:24018 RADLEX:RID3927 SNOMEDCT:21350002 RGO:24019 neuroepithelial cyst RGO:24019 PNET HP:0030065 SNOMEDCT:39781001 SNOMEDCT:699028006 RGO:24020 primitive neuroectodermal tumor RGO:24020 RGO:24021 quadrigeminal body neoplasm RGO:24021 DOID:6098 RGO:24022 thalamic neoplasm RGO:24022 RGO:24023 posterior hypothalamic neoplasm RGO:24023 RGO:24024 brainstem neoplasm RGO:24024 RGO:24025 tectal plate neoplasm RGO:24025 DOID:5553 RGO:24026 pineal choriocarcinoma RGO:24026 DOID:4790 HP:0030071 ORDO:251883 RADLEX:RID4404 SNOMEDCT:39005004 SNOMEDCT:715903004 RGO:24028 medulloepithelioma RGO:24028 RGO:24029 pigmented medulloblastoma RGO:24029 DOID:0060104 HP:0007129 RGO:24030 cerebellar medulloblastoma RGO:24030 RGO:24031 lateral medulloblastoma RGO:24031 HP:0010796 RGO:24032 brainstem glioma RGO:24032 RGO:24035 pontine glioma RGO:24035 RGO:24036 choroid plexus tumor RGO:24036 RGO:24037 cerebellar neoplasm RGO:24037 RGO:24038 acute infarction RGO:24038 RGO:24040 irregular foramen magnum RGO:24040 RGO:24042 bilateral fusion of C1 to base of skull RGO:24042 RGO:24043 unilateral fusion of C1 to base of skull RGO:24043 RGO:24044 skull base tumor RGO:24044 RGO:24046 granulomatous infection RGO:24046 RGO:24047 basilar arachnoiditis RGO:24047 Chiari 1 Chiari I HP:0007099 ORDO:268882 RGO:24048 Chiari I malformation RGO:24048 Arnold-Chiari malformation ORDO:1136 RGO:24049 Chiari II malformation RGO:24049 RGO:24050 craniovertebral junction fusion deformity RGO:24050 RGO:24052 CSF overproduction RGO:24052 unilateral pulmonary hypoplasia ORDO:2258 RGO:24054 hypoplasia of one lung RGO:24054 RGO:24055 acute pleurisy RGO:24055 SNOMEDCT:35851005 RGO:24056 chronic empyema RGO:24056 DOID:106 RGO:24057 pleural tuberculosis RGO:24057 RGO:24058 ruptured liver RGO:24058 RGO:24059 subphrenic hematoma RGO:24059 HP:0006597 SNOMEDCT:64228003 RGO:24061 diaphragmatic paralysis RGO:24061 RGO:24063 primary mediastinal malignancy RGO:24063 RGO:24065 surgical transection RGO:24065 RGO:24066 metastatic mediastinal malignancy RGO:24066 RGO:24068 normal newborn RGO:24068 SNOMEDCT:395507008 RGO:24069 premature infant RGO:24069 discogenic sclerosis DOID:2247 ICD10CM:M47 RADLEX:RID5121 SNOMEDCT:8847002 RGO:24071 spondylosis RGO:24071 RGO:24074 osteolytic osteosarcoma RGO:24074 RGO:24075 notochordal rest RGO:24075 RGO:24076 metastasis to sacrum RGO:24076 DOID:263 SNOMEDCT:363518003 RGO:24079 renal cancer RGO:24079 ORDO:97286 RGO:24082 Carney-Stratakis syndrome RGO:24082 RGO:24083 familial GIST syndrome RGO:24083 HP:0031474 RGO:24084 pulmonary chondroma RGO:24084 RGO:24085 gastric GIST RGO:24085 RGO:24086 infantile osteopetrosis RGO:24086 RGO:24087 infantile hydrocephalus RGO:24087 SNOMEDCT:124297004 RGO:24088 hexokinase deficiency RGO:24088 glucose-6-phosphate dehydrogenase deficiency RGO:24089 G6PD deficiency RGO:24089 RGO:24091 postshunting RGO:24091 HP:0012641 SNOMEDCT:277657001 RGO:24095 decreased intracranial pressure RGO:24095 SNOMEDCT:258593008 RGO:24096 ventricular shunt RGO:24096 RGO:24097 vestigial sella RGO:24097 RGO:24098 pituitary fossa tumor RGO:24098 RGO:24099 chromophobe pituitary adenoma RGO:24099 RGO:24100 eosinophilic pituitary adenoma RGO:24100 RGO:24102 juxtasellar neoplasm RGO:24102 RGO:24103 suprasellar neoplasm RGO:24103 SNOMEDCT:34420000 RGO:24105 storage disease RGO:24105 RGO:24106 spondylodiskitis RGO:24106 SNOMEDCT:26250004 RGO:24108 brucella RGO:24108 SNOMEDCT:3218000 RGO:24109 fungal infection RGO:24109 RGO:24110 dilated azygos system RGO:24110 RGO:24112 posterior mediastinal neoplasm RGO:24112 RGO:24113 primary vertebral neoplasm RGO:24113 spondylosis deformans SNOMEDCT:68859000 RGO:24114 spinal osteoarthritis RGO:24114 RGO:24115 extruded disk RGO:24115 SNOMEDCT:402843003 RGO:24120 venous lake RGO:24120 RGO:24121 diploic channel RGO:24121 RGO:24137 absent cranial convolutional markings RGO:24137 RGO:24138 benign subdural fluid collection of infancy RGO:24138 RGO:24139 tumor adjacent to calvarium RGO:24139 RGO:24140 subarachnoid cyst adjacent to calvarium RGO:24140 RGO:24141 familial microencephaly RGO:24141 HP:0011320 RGO:24142 unilateral lambdoid craniosynostosis RGO:24142 HP:0001357 ICD10CM:Q67.3 RADLEX:RID5417 SNOMEDCT:21850008 RGO:24143 plagiocephaly RGO:24143 HP:0011315 RGO:24144 unilateral coronal craniosynostosis RGO:24144 deformational plagiocephaly flathead syndrome postural skull flattening HP:0001357 SNOMEDCT:254024005 RGO:24145 positional plagiocephaly RGO:24145 RGO:24149 idiopathic craniosynostosis RGO:24149 RGO:24151 chromosome 7:del(7p) syndrome RGO:24151 RGO:24152 chromosome 7:dup(7q) syndrome RGO:24152 HP:0000248 RADLEX:RID5412 SNOMEDCT:13649004 RGO:24153 brachycephaly RGO:24153 SNOMEDCT:248379009 RGO:24154 short skull RGO:24154 HP:0002682 SNOMEDCT:13649004 RGO:24155 wide skull RGO:24155 RGO:24156 slightly high head RGO:24156 RGO:24157 harlequin orbits RGO:24157 RGO:24158 bilateral coronal suture fusion RGO:24158 RGO:24160 tall, wide, short head RGO:24160 RGO:24161 bilateral lambdoid and coronal suture fusion RGO:24161 HP:0000262 RADLEX:RID5419 SNOMEDCT:48069004 RGO:24162 turricephaly RGO:24162 RGO:24163 tower-shaped head RGO:24163 HP:0030799 RADLEX:RID5418 SNOMEDCT:4191007 RGO:24164 scaphocephaly RGO:24164 HP:0000268 ICD10CM:Q67.2 SNOMEDCT:72239002 RGO:24165 dolichocephaly RGO:24165 ORDO:991 RGO:24169 PAGOD syndrome RGO:24169 SNOMEDCT:57325008 RGO:24172 isoimmunization RGO:24172 ORDO:766 SNOMEDCT:74703006 RGO:24173 pyruvate kinase deficiency anemia RGO:24173 DOID:4371 ORDO:37748 SNOMEDCT:402415001 RGO:24174 Schnitzler syndrome RGO:24174 RGO:24175 repeated infection RGO:24175 RGO:24176 eczematous skin lesions RGO:24176 HP:0001974 SNOMEDCT:111583006 SNOMEDCT:414478003 RGO:24177 leukocytosis RGO:24177 RGO:24178 COACH syndrome RGO:24178 TRAP sequence TRAP syndrome acardiac fetus SNOMEDCT:205834002 RGO:24179 acardia RGO:24179 RGO:24180 chromosome 14 uniparental disomy RGO:24180 RGO:24181 Lin-Gettig syndrome RGO:24181 ORR syndrome RGO:24185 omphalocele-absent radial ray syndrome RGO:24185 RGO:24186 absent radial ray RGO:24186 SNOMEDCT:325325006 SNOMEDCT:395831005 RGO:24187 carbimazole RGO:24187 RGO:24188 chronic pseudomalignant lymphadenopathy RGO:24188 DOID:0060827 SNOMEDCT:702356009 RGO:24190 PPM-X syndrome RGO:24190 DOID:2468 SNOMEDCT:69322001 RGO:24191 psychotic disorder RGO:24191 RGO:24192 trisomy 1 syndrome RGO:24192 RGO:24193 chromosome 18p2 syndrome RGO:24193 DOID:0060235 ORDO:157 SNOMEDCT:238002005 RGO:24196 carnitine palmitoyltransferase II deficiency RGO:24196 HP:0010564 SNOMEDCT:232412004 RGO:24198 bifid epiglottis RGO:24198 DOID:0060485 ORDO:2152 SNOMEDCT:703535000 RGO:24200 Mowat-Wilson syndrome RGO:24200 DOID:0060305 HP:0000485 SNOMEDCT:268158009 RGO:24205 megalocornea RGO:24205 HP:0001270 SNOMEDCT:398991009 RGO:24206 motor retardation RGO:24206 DOID:0002116 HP:0001059 SNOMEDCT:77489003 RGO:24207 pterygium RGO:24207 RGO:24212 acardius anceps RGO:24212 RGO:24213 acardius acephalus RGO:24213 RGO:24214 acardius acormus RGO:24214 RGO:24215 acardius amorphus RGO:24215 spondylarthritis SNOMEDCT:371082009 RGO:24217 spondyloarthritis RGO:24217 DDD RADLEX:RID5086 RGO:24218 degenerative disk disease RGO:24218 RGO:24220 flexion-rotation injury RGO:24220 RGO:24221 hyperextension spinal injury RGO:24221 RGO:24222 endplate infarction RGO:24222 RGO:24225 vertebral osteomyelitis RGO:24225 RGO:24229 lymphangioma of tongue RGO:24229 RGO:24230 congenital tongue enlargement RGO:24230 ORDO:2430 RGO:24231 congenital macroglossia RGO:24231 RGO:24232 facial hemihypertrophy RGO:24232 RGO:24233 unilateral prognathism RGO:24233 TMJ syndrome SNOMEDCT:41888000 RGO:24234 temporomandibular joint syndrome RGO:24234 RGO:24236 erosive arthritis RGO:24236 RGO:24237 abnormal mandibular condyle RGO:24237 RGO:24238 abnormal mandibular condylar excursion RGO:24238 RGO:24239 TMJ steroid injections RGO:24239 HP:0012730 RGO:24240 absence of tongue RGO:24240 RGO:24241 severe hypoplasia of tongue RGO:24241 RGO:24242 acrofacial dysostosis Nager type RGO:24242 RGO:24243 acrofacial dysostosis Miller type RGO:24243 ORDO:952 RGO:24244 acrofacial dysostosis Weyers type RGO:24244 RGO:24246 idiopathic hyperdontia RGO:24246 SNOMEDCT:363505006 RGO:24247 mouth cancer RGO:24247 DOID:216 HP:0000670 ICD10CM:K02 SNOMEDCT:80967001 RGO:24249 dental caries RGO:24249 RGO:24250 hemangioma of mandible RGO:24250 RGO:24251 lymphangioma of mandible RGO:24251 DOID:824 HP:0000704 SNOMEDCT:41565005 RGO:24252 periodontitis RGO:24252 SNOMEDCT:196341005 RGO:24253 periapical abscess RGO:24253 KCOT OKC keratocystic odontogenic tumor RGO:24258 odontogenic keratocyst RGO:24258 ICD10CM:K09.0 SNOMEDCT:25418001 RGO:24259 primordial cyst RGO:24259 RGO:24261 congenital adontia RGO:24261 HP:0000327 ICD10CM:M26.02 RGO:24263 maxillary hypoplasia RGO:24263 RGO:24264 malar-zygomatic hypoplasia RGO:24264 RGO:24266 widened periodontal membrane RGO:24266 RGO:24267 idiopathic pulmonary ossification RGO:24267 DOID:12118 SNOMEDCT:40527005 RGO:24268 pulmonary hemosiderosis RGO:24268 Ceelen syndrome DOID:12118 ICD10CM:J84.03 ORDO:99931 SNOMEDCT:40527005 RGO:24269 idiopathic pulmonary hemosiderosis RGO:24269 RGO:24271 tracheobronchial cartilage calcification RGO:24271 RGO:24274 excessive calcium administration RGO:24274 RGO:24275 fluid-filled esophagus RGO:24275 DOID:4889 SNOMEDCT:10893003 RGO:24276 tuberculous lymphadenopathy RGO:24276 RGO:24278 subclavian artery anomaly RGO:24278 RGO:24279 thymic rebound RGO:24279 RGO:24282 normal infant thymus RGO:24282 RGO:24283 normal epicardial fat pad RGO:24283 aneurysm of ascending aorta ascending aortic aneurysm HP:0002631 RGO:24284 ascending aorta aneurysm RGO:24284 RGO:24289 chromosome 13:del(13q) syndrome RGO:24289 RGO:24290 caudal duplication syndrome RGO:24290 SNOMEDCT:20944008 RGO:24291 congenital scoliosis RGO:24291 RGO:24293 uterus didelphys-renal anomaly syndrome RGO:24293 RADLEX:RID3701 RGO:24294 ventriculitis RGO:24294 RGO:24295 hypoxic ischemic injury RGO:24295 RGO:24296 caudothalamic groove RGO:24296 RGO:24297 corpus callosum agenesis with midline cyst RGO:24297 SNOMEDCT:75132008 RGO:24298 parasitic cyst RGO:24298 RGO:24299 embryonal cell tumor RGO:24299 RGO:24300 dural sarcoma RGO:24300 DOID:4992 HP:0009734 SNOMEDCT:254976006 RGO:24301 optic nerve glioma RGO:24301 RGO:24302 pineal glioma RGO:24302 RGO:24303 parasitic RGO:24303 RADLEX:RID34413 SNOMEDCT:75934005 RGO:24304 metabolic disease RGO:24304 DOID:1289 RADLEX:RID5043 RGO:24305 degenerative disease RGO:24305 RADLEX:RID10404 SNOMEDCT:122463005 RGO:24308 embolization RGO:24308 RGO:24309 premature closure of sutures RGO:24309 RGO:24310 congenital scalp defect RGO:24310 ORDO:90350 RGO:24312 cutis laxa type 2 RGO:24312 RGO:24313 prenatal infection RGO:24313 HP:0001622 RGO:24314 premature birth RGO:24314 neuraminidase deficiency sialidosis RGO:24315 mucolipidosis type 1 RGO:24315 RGO:24317 chronic cyanotic congenital heart disease RGO:24317 RGO:24318 calvarial doughnut RGO:24318 RGO:24319 skull fracture RGO:24319 SNOMEDCT:110405005 SNOMEDCT:67864003 RGO:24320 burr hole RGO:24320 RGO:24321 craniotomy flap RGO:24321 RGO:24322 enlarged emissary channel RGO:24322 RADLEX:RID34480 SNOMEDCT:11240000 SNOMEDCT:138470007 RGO:24323 parietal foramen RGO:24323 RGO:24325 staphylococcal osteomyelitis RGO:24325 RGO:24326 electric burn RGO:24326 RGO:24328 osteonecrosis of skull RGO:24328 SNOMEDCT:105594005 SNOMEDCT:314534006 RGO:24330 thermal burn RGO:24330 RGO:24331 paranasal sinus carcinoma RGO:24331 RGO:24332 scalp carcinoma RGO:24332 RGO:24333 rodent ulcer of scalp RGO:24333 RGO:24336 cervical spine flexion injury RGO:24336 RGO:24337 cervical spine flexion-rotation injury RGO:24337 RGO:24342 anterior subluxation of cervical spine RGO:24342 RGO:24344 torn transverse spinal ligaments RGO:24344 RGO:24345 laxity of transverse spinal ligaments RGO:24345 DOID:6196 RGO:24346 Reiter/reactive arthritis RGO:24346 RGO:24347 erosion of odontoid RGO:24347 RGO:24348 absent odontoid process RGO:24348 HP:0003311 RGO:24349 hypoplastic odontoid process RGO:24349 RGO:24350 retropharyngeal infection RGO:24350 DOID:10301 HP:0011850 ICD10CM:K11.2 RADLEX:RID3533 SNOMEDCT:14756005 RGO:24351 parotitis RGO:24351 DOID:4637 SNOMEDCT:3502005 RGO:24352 cervical adenitis RGO:24352 HP:0030757 SNOMEDCT:299709002 RGO:24353 tooth abscess RGO:24353 RGO:24354 nasopharyngeal infection RGO:24354 DOID:9072 ICD10CM:M31.2 SNOMEDCT:58961005 RGO:24355 lethal midline granuloma RGO:24355 RGO:24356 nasal T-cell lymphoma RGO:24356 SNOMEDCT:25353009 RGO:24357 craniotomy RGO:24357 HP:0002816 ORDO:295229 RGO:24361 genu recurvatum RGO:24361 RGO:24362 sclerosing cemental mass RGO:24362 pulmonary infiltrate with eosinophilia RGO:24364 PIE RGO:24364 RGO:24366 hereditary short thumbs RGO:24366 RGO:24368 moldy hay RGO:24368 RGO:24369 wheat dust RGO:24369 RGO:24370 tabacosis RGO:24370 ORDO:98843 RGO:24371 nodular sclerosing Hodgkin lymphoma RGO:24371 Erionite RGO:24372 zeolite inhalation RGO:24372 RGO:24374 GCSF therapy RGO:24374 HP:0006289 RGO:24377 missing central incisors RGO:24377 HP:0011817 ORDO:268829 RGO:24378 basal encephalocele RGO:24378 RGO:24379 transsphenoid encephalocele RGO:24379 RGO:24380 maxillary antral lavage RGO:24380 RGO:24381 nasal packing for epistaxis RGO:24381 RGO:24382 indwelling nasogastric tube RGO:24382 DOID:1350 HP:0030072 RGO:24383 paranasal sinus neoplasm RGO:24383 RGO:24384 lingual cyst RGO:24384 RGO:24388 familial macroglossia RGO:24388 RGO:24390 calcified hepatic vein thrombus RGO:24390 CGD chronic granulomatous disease RGO:24392 chronic granulomatous disease of childhood RGO:24392 DOID:8566 SNOMEDCT:88594005 RGO:24393 herpes simplex infection RGO:24393 RGO:24394 Ischemic hepatic necrosis RGO:24394 DOID:9790 ICD10CM:B83.0 RGO:24395 visceral larva migrans RGO:24395 RGO:24396 chronic malnutrition RGO:24396 RGO:24397 growth hormone therapy RGO:24397 ICD10CM:B15 SNOMEDCT:25102003 RGO:24398 acute hepatitis A RGO:24398 RGO:24399 pancreatic ductal obstruction RGO:24399 HP:0002155 SNOMEDCT:302870006 RGO:24400 hypertriglyceridemia RGO:24400 HP:0002045 ICD10CM:T68 RADLEX:RID34682 SNOMEDCT:386689009 RGO:24401 hypothermia RGO:24401 RGO:24402 idiopathic pancreatitis RGO:24402 RGO:24403 penetrating peptic ulcer RGO:24403 DOID:4988 SNOMEDCT:445507008 RGO:24404 alcoholic pancreatitis RGO:24404 SNOMEDCT:23079006 SNOMEDCT:387126006 RGO:24405 vincristine RGO:24405 RGO:24406 glycogen storage disease type 1a RGO:24406 RGO:24407 pancreatobiliary duct anomaly RGO:24407 RGO:24408 meniscal tear RGO:24408 RGO:24409 cruciate tear RGO:24409 RGO:24410 intraarticular loose body RGO:24410 RADLEX:RID3636 SNOMEDCT:431631000124102 RGO:24411 granulomatous synovitis RGO:24411 RGO:24412 periarticular exostosis RGO:24412 RGO:24413 periarticular synostosis RGO:24413 retained fetal lung fluid RGO:24414 retained fetal alveolar fluid RGO:24414 RGO:24415 aspiration of amniotic fluid RGO:24415 SNOMEDCT:278927005 RGO:24416 aspiration of meconium RGO:24416 RGO:24417 osteomyelitis of spine with abscess RGO:24417 RGO:24419 dense vertebrae RGO:24419 HP:0003316 RGO:24420 butterfly vertebrae RGO:24420 RGO:24421 thoracic vertebral hypoplasia RGO:24421 RGO:24422 sagittal cleft vertebra RGO:24422 RGO:24424 lumbar vertebral fusion RGO:24424 RGO:24425 hypoplastic cervical spine RGO:24425 RGO:24429 chronic sclerosing osteomyelitis RGO:24429 DOID:13258 ORDO:99745 RGO:24431 typhoid RGO:24431 DOID:264 SNOMEDCT:84664004 RGO:24432 malignant hemangiopericytoma RGO:24432 RGO:24434 congenital salivary duct stricture RGO:24434 SNOMEDCT:275006003 RGO:24435 superficial parotidectomy RGO:24435 SNOMEDCT:13358001 RGO:24436 total parotidectomy RGO:24436 RGO:24437 bilateral intraparotid lymphadenopathy RGO:24437 RGO:24438 HIV-associated lymphoepithelial cysts RGO:24438 RGO:24439 bilateral parotid gland tumor RGO:24439 RGO:24442 lymphoepithelial parotid cysts RGO:24442 SNOMEDCT:19030005 RGO:24443 HIV RGO:24443 RGO:24445 reactive parotitis RGO:24445 RGO:24447 encapsulated exudate RGO:24447 RGO:24448 encapsulated pus RGO:24448 RGO:24449 encapsulated blood RGO:24449 DOID:1785 RGO:24451 pituitary neoplasm RGO:24451 RGO:24452 orbital neoplasm RGO:24452 SNOMEDCT:7300000 RGO:24453 lymphoepithelioma RGO:24453 RGO:24454 oral neoplasm RGO:24454 HP:0100630 RGO:24455 nasopharyngeal neoplasm RGO:24455 HP:0011079 SNOMEDCT:129263008 SNOMEDCT:235104008 RGO:24456 impacted tooth RGO:24456 ICD10CM:K09.1 SNOMEDCT:78753008 RGO:24457 globulomaxillary cyst RGO:24457 HP:0011068 RADLEX:RID4207 SNOMEDCT:79074005 RGO:24458 odontoma RGO:24458 polyps RADLEX:RID3881 SNOMEDCT:41329004 SNOMEDCT:441456002 RGO:24459 polyp RGO:24459 DOID:13444 ICD10CM:A24.0 SNOMEDCT:4639008 RGO:24460 glanders RGO:24460 RGO:24461 hypoplastic paranasal sinus RGO:24461 RGO:24462 absent paranasal sinus RGO:24462 RGO:24463 congenital sinus hypoplasia RGO:24463 RGO:24464 congenital sinus aplasia RGO:24464 RGO:24465 sinus neoplasm RGO:24465 RGO:24466 nonsecretory cyst RGO:24466 SNOMEDCT:11666007 RGO:24467 pyocele RGO:24467 RGO:24468 paranasal sinus hemorrhage RGO:24468 HP:0000421 ICD10CM:R04.0 SNOMEDCT:12441001 RGO:24469 epistaxis RGO:24469 SNOMEDCT:95353000 RGO:24470 mucosal edema RGO:24470 DOID:0050117 SNOMEDCT:40733004 RGO:24471 infectious disease RGO:24471 RGO:24473 absence of odontoid RGO:24473 RGO:24474 hypoplasia of odontoid RGO:24474 RGO:24475 fragmentation of odontoid RGO:24475 RGO:24476 infiltrating retinoblastoma RGO:24476 RGO:24478 varices with phleboliths RGO:24478 DOID:0060330 RGO:24497 Rapp-Hodgkin syndrome RGO:24497 ORDO:90339 RGO:24498 Rosselli-Gulienetti syndrome RGO:24498 RGO:24499 basal cell nevi RGO:24499 HP:0009755 ICD10CM:H02.52 SNOMEDCT:193953008 RGO:24502 ankyloblepharon RGO:24502 DOID:9296 HP:0410030 ICD10CM:Q36 SNOMEDCT:80281008 RGO:24504 cleft lip RGO:24504 DOID:9370 HP:0000520 SNOMEDCT:18265008 RGO:24505 exophthalmos RGO:24505 RGO:24506 congenital serous cyst RGO:24506 DOID:11212 ICD10CM:Q15.0 RGO:24509 hydrophthalmos RGO:24509 HP:0007035 RGO:24510 anterior encephalocele RGO:24510 RGO:24511 anterior meningocele RGO:24511 RGO:24513 severe hydrocephalus during growth period RGO:24513 HP:0011803 SNOMEDCT:204521002 RGO:24516 cleft nose RGO:24516 SNOMEDCT:7183006 RGO:24517 anophthalmos RGO:24517 RGO:24518 forebrain hypoplasia RGO:24518 RGO:24519 frontal sinus mucocele RGO:24519 HP:0007330 ICD10CM:Q01.0 ORDO:1931 SNOMEDCT:253103006 RGO:24520 frontal encephalocele RGO:24520 RGO:24521 antral cyst RGO:24521 RGO:24522 antral neoplasm RGO:24522 RGO:24523 supraglottic laryngeal carcinoma RGO:24523 SNOMEDCT:712648008 RGO:24524 epiglottic cyst RGO:24524 carcinoma of larynx DOID:2600 HP:0012118 SNOMEDCT:276975007 RGO:24525 laryngeal carcinoma RGO:24525 SNOMEDCT:372103002 RGO:24526 carcinoma of glottis RGO:24526 RADLEX:RID4357 SNOMEDCT:400149007 SNOMEDCT:421419001 SNOMEDCT:63629005 RGO:24527 lipoblastomatosis RGO:24527 RGO:24529 benign mixed salivary gland tumor RGO:24529 RADLEX:RID39169 RGO:24530 rotoscoliosis RGO:24530 RGO:24531 congenital thoracolumbar vertebral wedging RGO:24531 DOID:3025 RADLEX:RID3962 SNOMEDCT:45410002 RGO:24532 acinar cell carcinoma RGO:24532 RGO:24533 salivary gland calculus RGO:24533 RGO:24539 ganglioblastoma RGO:24539 SNOMEDCT:127018007 RGO:24540 thyroid tumor RGO:24540 SNOMEDCT:127020005 RGO:24541 parathyroid tumor RGO:24541 HP:0002886 SNOMEDCT:253030004 RGO:24542 glomus vagale tumor RGO:24542 SNOMEDCT:30699005 RGO:24543 carotid body tumor RGO:24543 RGO:24544 ectatic suprasellar segment of internal carotid artery RGO:24544 RGO:24545 ectatic cavernous segment of internal carotid artery RGO:24545 RGO:24546 cranial nerve III schwannoma RGO:24546 RGO:24547 cranial nerve IV schwannoma RGO:24547 RGO:24548 cranial nerve VI schwannoma RGO:24548 schwannoma of cranial nerve V RGO:24550 cranial nerve V schwannoma RGO:24550 HP:0012489 RGO:24552 suprasellar arachnoid cyst RGO:24552 RGO:24553 intrasellar arachnoid cyst RGO:24553 RGO:24554 infundibular metastasis RGO:24554 RGO:24555 optic nerve neurofibroma RGO:24555 RGO:24556 optic nerve meningioma RGO:24556 DOID:4968 ORDO:199244 SNOMEDCT:43019009 RGO:24557 Nelson syndrome RGO:24557 RGO:24558 primary precocious puberty RGO:24558 RGO:24560 adrenal ablation RGO:24560 RGO:24561 pituitary gland hypertrophy RGO:24561 RADLEX:RID3473 SNOMEDCT:61701006 RGO:24562 lymphocytic hypophysitis RGO:24562 RGO:24563 pituitary enlargement RGO:24563 RGO:24565 normal spine RGO:24565 RGO:24569 apophyseal joint malalignment RGO:24569 DOID:6682 HP:0003302 ICD10CM:M43.1 RADLEX:RID4780 SNOMEDCT:274152003 RGO:24570 spondylolisthesis RGO:24570 RGO:24571 congenital absence of contralateral posterior elements RGO:24571 RGO:24572 congenital hypoplasia of contralateral posterior elements RGO:24572 RGO:24573 intraspinal dermoid RGO:24573 RGO:24575 paranasal sinus mucocele RGO:24575 DOID:3565 RADLEX:RID4088 SNOMEDCT:127579001 RGO:24577 meningeal neoplasm RGO:24577 RGO:24578 primary malignant neoplasm of skull RGO:24578 RGO:24579 lesion of hard palate RGO:24579 RGO:24580 lesion of soft palate RGO:24580 RGO:24581 nasopharyngeal tumor RGO:24581 RGO:24582 hypopharyngeal tumor RGO:24582 SNOMEDCT:402929007 RGO:24583 bacterial cellulitis RGO:24583 acute necrotizing ulcerative gingivitis trench mouth DOID:13924 RGO:24584 Vincent angina RGO:24584 RGO:24585 nucleus pulposus degeneration RGO:24585 RGO:24586 metastasis to adjacent vertebra with vertebral collapse RGO:24586 SNOMEDCT:9631008 RGO:24587 rheumatoid spondylitis RGO:24587 HP:0002948 RADLEX:RID34797 SNOMEDCT:55705006 RGO:24588 spinal fusion RGO:24588 RGO:24589 congenital block vertebra RGO:24589 RGO:24591 postural flattening RGO:24591 RGO:24592 immobilized infant RGO:24592 RGO:24593 idiopathic bathrocephaly RGO:24593 SNOMEDCT:609528003 RGO:24594 posterior fossa arachnoid cyst RGO:24594 HP:0002436 SNOMEDCT:445468002 RGO:24595 occipital meningocele RGO:24595 RGO:24596 intradiploic dermoid cyst RGO:24596 RGO:24597 scalp cyst RGO:24597 RGO:24598 scalp neoplasm RGO:24598 RGO:24599 intracranial neoplasm with erosion of calvarium RGO:24599 RGO:24600 arteriovenous malformation of skull RGO:24600 RGO:24601 hemangioma of scalp RGO:24601 RGO:24602 arteriovenous malformation of scalp RGO:24602 RGO:24603 intradiploic hematoma RGO:24603 RGO:24604 cephalohydrocele RGO:24604 RGO:24606 senile parietal thinning RGO:24606 RGO:24607 bone flap necrosis RGO:24607 RGO:24608 leptomeningeal fibrosis RGO:24608 DOID:3872 SNOMEDCT:230156002 RGO:24609 meningeal carcinomatosis RGO:24609 fungus disease RGO:24611 fungal disease RGO:24611 RGO:24615 primary CNS tumor spread RGO:24615 DOID:3565 RGO:24616 primary meningeal tumor RGO:24616 RGO:24617 primary leptomeningeal glioblastomatosis RGO:24617 RGO:24619 localized meningitis RGO:24619 RGO:24627 occipital foramina RGO:24627 SNOMEDCT:126488004 RGO:24628 skin tumor RGO:24628 RGO:24629 scalp tumor RGO:24629 RGO:24630 compact osteoma RGO:24630 RGO:24631 soft tissue adenoma RGO:24631 RGO:24632 ceruminous gland tumor of external auditory canal RGO:24632 RGO:24633 carcinoma of external auditory canal RGO:24633 RGO:24634 multilocular radicular cyst RGO:24634 Stafne cyst RGO:24635 developmental lingual mandibular salivary gland defect RGO:24635 RGO:24637 ameloblastic myxoma RGO:24637 adenoameloblastoma RADLEX:RID4180 SNOMEDCT:60599006 RGO:24638 adenomatoid odontogenic tumor RGO:24638 HP:0000704 SNOMEDCT:271668009 RGO:24640 pyorrhea RGO:24640 RGO:24641 primary neoplasm RGO:24641 cancrum oris DOID:9672 ICD10CM:A69.0 ORDO:2700 SNOMEDCT:18116006 RGO:24642 noma RGO:24642 DOID:4617 HP:0000700 SNOMEDCT:81407003 RGO:24644 periapical granuloma RGO:24644 RGO:24645 metastasis to temporal bone RGO:24645 RGO:24646 parotid carcinoma RGO:24646 RGO:24647 cyst of papilla palatina RGO:24647 RGO:24649 median alveolar cyst RGO:24649 ICD10CM:K09.1 SNOMEDCT:64268004 RGO:24650 median palatal cyst RGO:24650 RGO:24652 surgical ciliated cyst of maxillary sinus RGO:24652 nasopalatine canal cyst nasopalatine duct cyst SNOMEDCT:4749004 RGO:24653 incisive canal cyst RGO:24653 ICD10CM:K09.1 SNOMEDCT:90516007 RGO:24655 nasolabial cyst RGO:24655 DOID:2562 HP:0030757 SNOMEDCT:196341005 RGO:24657 dentoalveolar abscess RGO:24657 RGO:24658 hyperplasia of maxillary sinus lining RGO:24658 RGO:24660 malignant salivary gland tumor RGO:24660 RGO:24661 midpalatal cyst RGO:24661 RGO:24662 focal cementoosseous dysplasia RGO:24662 HP:0100789 ICD10CM:M27.0 SNOMEDCT:46752004 RGO:24663 torus palatinus RGO:24663 ICD10CM:M27.0 SNOMEDCT:11625007 RGO:24664 torus mandibularis RGO:24664 RADLEX:RID3526 SNOMEDCT:55413008 RGO:24665 condensing osteitis RGO:24665 DOID:10788 SNOMEDCT:55413008 RGO:24666 sclerosing osteitis RGO:24666 ICD10CM:S06 SNOMEDCT:127296001 RGO:24667 intracranial injury RGO:24667 DOID:10554 ICD10CM:A69.22 RADLEX:RID3499 SNOMEDCT:7125002 RGO:24668 meningoencephalitis RGO:24668 RGO:24669 malignant skull neoplasm RGO:24669 RGO:24670 lymphoepithelioma of paranasal sinus RGO:24670 RGO:24671 lymphoepithelioma of nasopharynx RGO:24671 RGO:24672 chronic nasopharyngeal infection RGO:24672 DOID:10755 ICD10CM:H70.22 SNOMEDCT:28593007 RGO:24673 chronic petrositis RGO:24673 DOID:10794 RGO:24674 sphenoid sinusitis RGO:24674 RGO:24675 healing vitamin D-resistant rickets RGO:24675 RGO:24676 chronic scalp cellulitis RGO:24676 RGO:24677 sutural sclerosis RGO:24677 SNOMEDCT:139582005 SNOMEDCT:61918000 RGO:24678 external occipital protuberance RGO:24678 RADLEX:RID5172 SNOMEDCT:86217007 RGO:24679 ischemic necrosis RGO:24679 SNOMEDCT:416536005 SNOMEDCT:416744008 RGO:24680 bone flap RGO:24680 RGO:24681 treated brown tumor of hyperparathyroidism RGO:24681 RGO:24682 hydantoin therapy RGO:24682 RGO:24683 cerebral atrophy in childhood RGO:24683 RGO:24684 hemihypertrophy of cranium RGO:24684 RGO:24685 hyperostosis interna generalisata RGO:24685 ORDO:77296 RGO:24686 Morgagni-Stewart-Morel syndrome RGO:24686 RGO:24687 treated rickets RGO:24687 RGO:24688 post-shunt hydrocephalus RGO:24688 RGO:24690 cranial nerve VII schwannoma RGO:24690 schwannoma of cranial nerve IX RGO:24691 cranial nerve IX schwannoma RGO:24691 schwannoma of cranial nerve X RGO:24692 cranial nerve X schwannoma RGO:24692 RGO:24693 cranial nerve XI schwannoma RGO:24693 RGO:24694 cranial nerve XII schwannoma RGO:24694 RGO:24695 meningioma of petrous apex RGO:24695 RGO:24696 aneurysm of internal auditory canal artery RGO:24696 RGO:24697 aneurysm of intrapetrous carotid artery RGO:24697 RGO:24698 aneurysm of intracavernous carotid artery RGO:24698 RGO:24699 spinal cord hematoma RGO:24699 RGO:24700 spinal cord contusion RGO:24700 RGO:24701 spinal cord edema RGO:24701 RGO:24702 metastatic medulloblastoma RGO:24702 RGO:24703 spinal cord infarction RGO:24703 RGO:24705 anterior spinal artery occlusion RGO:24705 RGO:24706 occlusion of spinal vein RGO:24706 RGO:24707 spinal abscess RGO:24707 DOID:322 HP:0012486 RADLEX:RID3501 SNOMEDCT:41370002 RGO:24708 myelitis RGO:24708 RGO:24710 hematic cyst RGO:24710 RGO:24711 optic nerve schwannoma RGO:24711 RGO:24712 neurofibroma of cranial nerve III RGO:24712 RGO:24713 neurofibroma of cranial nerve IV RGO:24713 RGO:24714 neurofibroma of cranial nerve V RGO:24714 ICD10CM:H31.4 RADLEX:RID4773 SNOMEDCT:27871007 RGO:24716 choroidal detachment RGO:24716 DOID:9669 ICD10CM:H25 SNOMEDCT:39450006 RGO:24717 senile cataract RGO:24717 RGO:24719 chronic posttraumatic degeneration RGO:24719 HP:0031035 RGO:24720 chronic infection RGO:24720 RGO:24722 optic nerve ischemia RGO:24722 RGO:24724 severe hypertension RGO:24724 DOID:13375 RADLEX:RID3687 SNOMEDCT:400130008 RGO:24725 temporal arteritis RGO:24725 RGO:24726 systemic vasculopathy RGO:24726 RGO:24727 HIV-related optic neuropathy RGO:24727 DOID:3565 HP:0100009 SNOMEDCT:302820008 RGO:24728 intracranial meningioma RGO:24728 RGO:24729 compensatory hypertrophy with contralateral neural arch deficiency RGO:24729 RGO:24731 destruction of neural arch RGO:24731 RGO:24732 destruction of pedicle RGO:24732 RGO:24735 congenitally absent vertebral pedicle RGO:24735 RGO:24736 congenitally hypoplastic vertebral pedicle RGO:24736 RGO:24737 absent vertebral pedicle RGO:24737 HP:0030278 RGO:24738 hypoplastic vertebral pedicle RGO:24738 RGO:24739 vertebral artery tortuosity RGO:24739 RGO:24740 bulging intervertebral disk RGO:24740 RGO:24741 herniated nucleus pulposus RGO:24741 RGO:24742 sequestered nucleus pulposus RGO:24742 RGO:24743 epidural scar RGO:24743 RGO:24744 interverbebral disk surgery RGO:24744 HP:0100790 RADLEX:RID4895 SNOMEDCT:414403008 SNOMEDCT:52515009 RGO:24748 hernia RGO:24748 RGO:24749 caudal dysplasia RGO:24749 Greenberg dysplasia hydrops-ectopic calcification-moth-eaten appearance dysplasia RGO:24751 hydrops - ectopic calcification - moth-eaten skeletal dysplasia RGO:24751 ICD10CM:D69.41 ORDO:1959 SNOMEDCT:75331009 RGO:24754 Evans syndrome RGO:24754 RGO:24755 ovarian dermoid cyst-autoimmune hemolytic anemia syndrome RGO:24755 RGO:24756 CATCH 22 syndrome RGO:24756 RGO:24757 familial hypomagnesemia RGO:24757 SNOMEDCT:71858003 RGO:24758 autoimmune hypoglycemia RGO:24758 Kabuki makeup syndrome Niikawa-Kuroki syndrome DOID:0060473 ORDO:2322 RGO:24759 Kabuki syndrome RGO:24759 RGO:24760 postprandial reactive hypoglycemia RGO:24760 RGO:24761 beer potomania syndrome RGO:24761 SNOMEDCT:427698009 RGO:24762 refeeding syndrome RGO:24762 ORDO:1920 RGO:24763 toluene embryopathy RGO:24763 RGO:24764 chromosome 11q- syndrome RGO:24764 ORDO:3322 SNOMEDCT:707276009 RGO:24766 Hoyeraal-Hreidarsson syndrome RGO:24766 HP:0012156 SNOMEDCT:61070002 RGO:24767 hemophagocytosis RGO:24767 HP:0002079 RGO:24770 corpus callosum hypoplasia RGO:24770 HP:0012448 SNOMEDCT:135810007 RGO:24771 delayed myelination RGO:24771 SNOMEDCT:241975000 RGO:24772 chronic mountain sickness RGO:24772 DOID:0060652 ORDO:90042 RGO:24774 primary familial and congenital polycythemia RGO:24774 RGO:24775 2,3-DPGP deficiency RGO:24775 DOID:4674 ICD10CM:E34.5 ORDO:754 SNOMEDCT:12313004 RGO:24776 androgen insensitivity syndrome RGO:24776 DOID:0050885 ORDO:85173 SNOMEDCT:702384004 RGO:24779 IMAGe syndrome RGO:24779 ORDO:2789 RGO:24782 lateral meningocele syndrome RGO:24782 DOID:0060306 SNOMEDCT:703508009 RGO:24783 Meier-Gorlin syndrome RGO:24783 HP:0000835 RGO:24785 adrenal hypoplasia RGO:24785 ORDO:2008 RGO:24786 acro-cardio-facial syndrome RGO:24786 ORDO:1112 RGO:24787 aphalangy - hemivertebrae - urogenital-intestinal dysgenesis syndrome RGO:24787 Nivelon-Nivelon-Mabille syndrome chondrodysplasia - disorder of sex development ORDO:1422 RGO:24788 chondrodysplasia-pseudohermaphrodism RGO:24788 RGO:24791 Du Pan-like syndrome RGO:24791 ORDO:1475 RGO:24793 renal-coloboma syndrome RGO:24793 RGO:24794 valproic acid embryopathy RGO:24794 RGO:24795 Müllerian dysgenesis RGO:24795 RGO:24797 chromosome 20p- syndrome RGO:24797 SNOMEDCT:253851000 RGO:24798 diphallus RGO:24798 RGO:24800 MR syndrome RGO:24800 RADLEX:RID5986 RGO:24801 tumor vascularity RGO:24801 RGO:24802 tumor encasement RGO:24802 RGO:24803 decreased pCO RGO:24803 RADLEX:RID4962 SNOMEDCT:257885003 SNOMEDCT:26036001 RGO:24804 occlusion RGO:24804 RGO:24805 brain contusion RGO:24805 DOID:1826 HP:0001250 SNOMEDCT:84757009 RGO:24806 epilepsy RGO:24806 SNOMEDCT:708039003 RGO:24807 inflammatory lesion RGO:24807 SNOMEDCT:372087000 RGO:24808 primary malignant neoplasm RGO:24808 RGO:24809 epidural hygroma RGO:24809 RGO:24810 avascular meningioma RGO:24810 SNOMEDCT:428954009 RGO:24811 low grade glioma RGO:24811 RGO:24815 steal phenomenon RGO:24815 RGO:24816 normal large subarachnoid space RGO:24816 RGO:24817 dissecting thoracic aortic aneurysm RGO:24817 RGO:24818 brachiocephalic artery occlusion RGO:24818 RGO:24819 brachiocephalic artery stenosis RGO:24819 RGO:24820 neck trauma RGO:24820 RGO:24824 extravascular obstruction RGO:24824 RGO:24825 subclavian artery hypoplasia RGO:24825 RGO:24826 subclavian artery atresia RGO:24826 RGO:24827 tetralogy of Fallot correction RGO:24827 RGO:24828 coarctation of aorta correction RGO:24828 SNOMEDCT:262689001 RGO:24829 cerebral contusion RGO:24829 HP:0001342 SNOMEDCT:274100004 RGO:24830 cerebral hemorrhage RGO:24830 HP:0100310 SNOMEDCT:428268007 RGO:24833 extradural hematoma RGO:24833 subdural subdural hemorrhage RADLEX:RID4706 SNOMEDCT:95453001 RGO:24834 subdural hematoma RGO:24834 RGO:24836 quadrigeminal cistern arachnoid cyst RGO:24836 RGO:24837 basal arachnoiditis RGO:24837 RGO:24838 cerebral maldevelopment RGO:24838 Miller-Dieker lissencephaly syndrome chromosome 17p13.3 deletion syndrome congenital agyria DOID:0060469 ICD10CM:Q93.88 ORDO:531 SNOMEDCT:253148005 RGO:24839 Miller-Dieker syndrome RGO:24839 RGO:24840 congenital aqueductal stenosis RGO:24840 RGO:24841 congenital aqueductal occlusion RGO:24841 DOID:13336 ICD10CM:P37.1 ORDO:858 SNOMEDCT:73893000 RGO:24842 congenital toxoplasmosis RGO:24842 RGO:24843 congenital cryptococcosis RGO:24843 DOID:640 RADLEX:RID3414 SNOMEDCT:62950007 RGO:24844 encephalomyelitis RGO:24844 RGO:24845 cortical venous thrombosis RGO:24845 HP:0030746 SNOMEDCT:23276006 RGO:24846 intraventricular hemorrhage RGO:24846 DOID:3772 RGO:24847 intraventricular meningioma RGO:24847 RGO:24848 tentorial meningioma RGO:24848 RGO:24849 acute meningitis RGO:24849 DOID:10341 ICD10CM:G03.1 SNOMEDCT:21664006 RGO:24850 chronic meningitis RGO:24850 RGO:24851 midbrain neoplasm RGO:24851 RGO:24852 midbrain hemorrhage RGO:24852 RGO:24854 gastrointestinal malignancy RGO:24854 RGO:24855 genitourinary malignancy RGO:24855 HP:0000388 RGO:24858 middle ear infection RGO:24858 DOID:9507 RGO:24859 ethmoid sinusitis RGO:24859 DOID:10791 SNOMEDCT:78737005 RGO:24860 frontal sinusitis RGO:24860 SNOMEDCT:36910002 RGO:24861 craniectomy RGO:24861 RGO:24862 inflammatory RGO:24862 DOID:1319 RGO:24864 primary brain neoplasm RGO:24864 RADLEX:RID28770 RGO:24865 intrathecal contrast RGO:24865 HP:0100250 RGO:24866 meningeal calcification RGO:24866 RGO:24867 postischemic meningeal hypervascularity RGO:24867 RGO:24868 gliomatosis RGO:24868 RGO:24870 seeding from primary neoplasm RGO:24870 RGO:24872 paranasal sinus surgery RGO:24872 RGO:24873 ventriculography RGO:24873 SNOMEDCT:52699005 RGO:24874 hypophysectomy RGO:24874 RGO:24875 neoplasm eroding base of skull RGO:24875 RADLEX:RID4633 SNOMEDCT:134222005 SNOMEDCT:262560006 RGO:24876 penetrating injury RGO:24876 RGO:24877 paranasal sinus fracture RGO:24877 SNOMEDCT:204049003 RGO:24878 cerebellar aplasia RGO:24878 HP:0001321 SNOMEDCT:16026008 RGO:24879 cerebellar hypoplasia RGO:24879 RGO:24881 Chiari III malformation RGO:24881 RGO:24883 infective emboli RGO:24883 RGO:24886 Parkinsonism-plus syndromes RGO:24886 ICD10CM:E71.522 ORDO:139399 SNOMEDCT:65389002 RGO:24887 adrenomyeloneuropathy RGO:24887 RGO:24888 Alper disease RGO:24888 DOID:3613 ORDO:141 RGO:24889 Canavan disease RGO:24889 mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes DOID:3687 ICD10CM:E88.41 ORDO:550 RGO:24890 MELAS syndrome RGO:24890 RGO:24894 acute encephalitis RGO:24894 RGO:24895 epidemic encephalopathies RGO:24895 RGO:24896 cerebral neoplasm RGO:24896 RADLEX:RID5056 RGO:24897 hypoxic-ischemic encephalopathy RGO:24897 RGO:24898 toxic RGO:24898 subcortical arteriosclerotic encephalopathy ORDO:1249 RADLEX:RID3295 RGO:24900 Binswanger disease RGO:24900 RGO:24901 postviral leukoencephalopathy RGO:24901 brain shearing injury shearing injury RADLEX:RID4644 RGO:24902 diffuse axonal injury RGO:24902 RGO:24904 whole brain radiation RGO:24904 RGO:24905 ependymitis granularis RGO:24905 RGO:24906 deep white matter ischemia RGO:24906 RGO:24907 subacute white matter encephalitis RGO:24907 RGO:24908 virchow-Robin spaces RGO:24908 RGO:24909 resolving hematoma RGO:24909 RGO:24912 acute hypotension RGO:24912 DOID:2030 HP:0000739 SNOMEDCT:48694002 RGO:24913 anxiety RGO:24913 RGO:24916 cortical vein occlusion RGO:24916 DOID:5162 SNOMEDCT:17941002 RGO:24917 arteriolosclerosis RGO:24917 HP:0030748 SNOMEDCT:276650005 RGO:24919 germinal matrix hemorrhage RGO:24919 RGO:24920 hemorrhagic infarction RGO:24920 RGO:24921 antral carcinoma RGO:24921 RGO:24922 nasal carcinoma RGO:24922 HP:0000452 SNOMEDCT:306963008 RGO:24923 choanal stenosis RGO:24923 RGO:24924 nasal septum congenital deformity RGO:24924 ORDO:141107 RGO:24925 mature nasopharyngeal teratoma RGO:24925 RGO:24926 transsphenoid encephalomeningocele RGO:24926 RGO:24928 nasal plate fracture RGO:24928 RGO:24929 nasal septum fracture RGO:24929 HP:0004646 RGO:24930 nasal bone hypoplasia RGO:24930 RGO:24931 inflammatory mucosal swelling RGO:24931 RGO:24932 allergic mucosal swelling RGO:24932 RGO:24933 traumatic mucosal swelling RGO:24933 RGO:24934 functional megacolon RGO:24934 HP:0025023 SNOMEDCT:91375006 RGO:24935 rectal atresia RGO:24935 RGO:24936 liver infarct RGO:24936 SNOMEDCT:387525002 SNOMEDCT:91667005 RGO:24939 hydrochlorothiazide RGO:24939 SNOMEDCT:32647002 SNOMEDCT:395975005 RGO:24940 ergotamine RGO:24940 RGO:24942 mesulergine RGO:24942 SNOMEDCT:373345002 SNOMEDCT:75959001 RGO:24944 tamoxifen RGO:24944 RGO:24945 nilutomide RGO:24945 SNOMEDCT:372745006 SNOMEDCT:45311002 RGO:24949 terbutaline RGO:24949 SNOMEDCT:372893009 SNOMEDCT:89785009 RGO:24950 ritodrine RGO:24950 SNOMEDCT:372818004 SNOMEDCT:68774008 RGO:24951 isoxsuprine RGO:24951 SNOMEDCT:13512003 SNOMEDCT:372653009 RGO:24953 minocycline RGO:24953 SNOMEDCT:12436009 SNOMEDCT:387051009 RGO:24954 vinblastine RGO:24954 SNOMEDCT:349851002 SNOMEDCT:409198005 RGO:24955 vindesine RGO:24955 SNOMEDCT:108792008 SNOMEDCT:372541004 RGO:24956 vinorelbine RGO:24956 ICD10CM:J34.89 SNOMEDCT:65034006 RGO:24959 rhinolith RGO:24959 RGO:24960 turbinate enlargement RGO:24960 SNOMEDCT:232360002 RGO:24961 concha bullosa RGO:24961 RGO:24962 maxillary sinus carcinoma RGO:24962 ICD10CM:T004 SNOMEDCT:23496000 SNOMEDCT:T004 RGO:24963 fungus RGO:24963 RGO:24965 angiomatous polyp RGO:24965 RGO:24966 nasoantral polyp RGO:24966 SNOMEDCT:232389000 RGO:24969 pott puffy tumor RGO:24969 DOID:0050904 RGO:24971 salivary gland carcinoma RGO:24971 RGO:24972 salivary gland mixed tumor RGO:24972 DOID:4545 RADLEX:RID4143 SNOMEDCT:56565002 RGO:24975 mesenchymal chondrosarcoma RGO:24975 RGO:24976 glomus jugulare paraganglioma RGO:24976 HP:0002886 RGO:24977 glomus vagale paraganglioma RGO:24977 RGO:24978 retropharyngeal cellulitis RGO:24978 RGO:24980 cervical spine lesion RGO:24980 DOID:6312 RGO:24981 clivus chordoma RGO:24981 RGO:24983 tonsils RGO:24983 enlarged adenoid DOID:0060311 HP:0040261 RGO:24986 adenoid hypertrophy RGO:24986 RGO:24987 malignant neoplasm RGO:24987 ICD10CM:J33 SNOMEDCT:52756005 RGO:24988 nasal polyp RGO:24988 RGO:24991 turbinate hypertrophy RGO:24991 DOID:4437 RGO:24992 skull base meningioma RGO:24992 RGO:24994 internal carotic artery aneurysm RGO:24994 RGO:24995 paraclinoid aneurysm RGO:24995 RGO:24996 hyperostotic bone disease RGO:24996 SNOMEDCT:27058005 RGO:24997 necrotizing granuloma RGO:24997 RGO:24998 chronic hypertrophic polypoid rhinosinusitis RGO:24998 RGO:24999 sphenoethmoid mucocele RGO:24999 SNOMEDCT:277185000 RGO:25000 trigeminal schwannoma RGO:25000 RGO:25001 perineural tumor extension RGO:25001 RGO:25002 pterygoid plate fracture RGO:25002 RGO:25004 odontogenic abscess RGO:25004 RGO:25005 denervation atrophy RGO:25005 RGO:25006 parapharyngeal cyst RGO:25006 RGO:25008 hypersomnolence states RGO:25008 RGO:25009 enlarged uvula RGO:25009 HP:0002459 SNOMEDCT:15241006 RGO:25010 dysautonomia RGO:25010 RGO:25011 mandible fracture RGO:25011 RGO:25012 soft tissues abscess RGO:25012 RGO:25013 thorotrast injury RGO:25013 RGO:25014 hypopharyngeal neoplasm RGO:25014 RGO:25015 oropharyngeal neoplasm RGO:25015 DOID:2275 HP:0025439 RADLEX:RID3539 SNOMEDCT:405737000 RGO:25016 pharyngitis RGO:25016 RGO:25017 parotid infection RGO:25017 RGO:25018 lateral pharyngeal diverticulum RGO:25018 HP:0006509 SNOMEDCT:14011008 RGO:25019 tracheal diverticulum RGO:25019 RADLEX:RID4819 SNOMEDCT:399291005 RGO:25020 Zenker diverticulum RGO:25020 RGO:25021 sternocleidomastoid muscle hypertrophy RGO:25021 RGO:25022 jugular vein asymmetry RGO:25022 RGO:25023 jugular vein ectasia RGO:25023 RGO:25024 external laryngocele RGO:25024 RGO:25025 ectopic salivary gland tissue RGO:25025 RGO:25027 paraproteinemias RGO:25027 RGO:25029 coagulation defects RGO:25029 RGO:25030 central venous line placement RGO:25030 RGO:25031 indwelling catheter placement RGO:25031 RGO:25032 intravenous drug abuse RGO:25032 RGO:25033 suppurative thrombophlebitis RGO:25033 surgical procedure RADLEX:RID1560 SNOMEDCT:257556004 RGO:25035 surgery RGO:25035 RGO:25036 intracranial venous sinus thrombus extension RGO:25036 SNOMEDCT:23290009 RGO:25039 adenomatous hyperplasia RGO:25039 DOID:6204 SNOMEDCT:55021007 RGO:25040 follicular adenoma RGO:25040 DOID:3113 SNOMEDCT:25910003 RGO:25041 papillary carcinoma RGO:25041 DOID:3962 SNOMEDCT:5257006 RGO:25042 follicular carcinoma RGO:25042 DOID:3974 RADLEX:RID4488 SNOMEDCT:32913002 RGO:25043 medullary carcinoma RGO:25043 SNOMEDCT:57596004 RGO:25044 Hürthle cell carcinoma RGO:25044 RGO:25045 cystic thyroid nodule RGO:25045 RADLEX:RID49690 SNOMEDCT:367644007 RGO:25046 simple cyst RGO:25046 RGO:25048 cystic parathyroid adenoma RGO:25048 SNOMEDCT:25476006 RGO:25049 acute suppurative thyroiditis RGO:25049 Riedel struma ICD10CM:E06.5 ORDO:64744 RADLEX:RID3670 SNOMEDCT:89024000 RGO:25050 Riedel thyroiditis RGO:25050 RGO:25051 radiation-induced thyroiditis RGO:25051 acute panniculitis DOID:3928 RGO:25053 Dercum disease RGO:25053 SNOMEDCT:253596003 RGO:25055 absent pulmonary valve syndrome RGO:25055 RGO:25056 Beemer lethal malformation syndrome RGO:25056 RGO:25057 cardioauditory syndrome RGO:25057 Forney-Robinson-Pascoe syndrome cardiospondylocarpofacial syndrome mitral regurgitation - deafness - skeletal anomalies RGO:25058 Forney syndrome RGO:25058 RGO:25061 cardioskeletal syndrome Kuwaiti type RGO:25061 SNOMEDCT:715987000 RGO:25064 Sonoda syndrome RGO:25064 CTAF RGO:25065 conotruncal anomaly face syndrome RGO:25065 RGO:25070 familial atrial septal defect with prolonged atrioventricular conduction RGO:25070 RGO:25071 familial atrioventricular septal defect RGO:25071 RGO:25072 familial brachydactyly type E and atrial septal defect RGO:25072 ORDO:2445 RGO:25073 familial conotruncal malformation RGO:25073 RGO:25074 familial Ebstein anomaly RGO:25074 DOID:14679 ORDO:887 RGO:25075 VACTERL association RGO:25075 RGO:25077 web neck anomaly RGO:25077 ORDO:3191 RGO:25079 subaortic stenosis short stature syndrome RGO:25079 RGO:25080 sternal-cardiac malformation association RGO:25080 ORDO:99063 SNOMEDCT:41371000119100 RGO:25081 Shone complex RGO:25081 ORDO:96167 RGO:25082 recombinant 8 syndrome RGO:25082 RGO:25083 Örstavik-Lindemann-Solberg syndrome RGO:25083 RGO:25085 primary hypertrophic osteoathropathy RGO:25085 ORDO:2351 RGO:25087 Kousseff syndrome RGO:25087 RGO:25088 Jones-Waldman syndrome RGO:25088 RGO:25090 familial short stature, small hands, and valvular heart disease RGO:25090 RGO:25091 tricuspid atresia and annular hypoplasia RGO:25091 RGO:25092 familial subaortic membranous stenosis RGO:25092 RGO:25093 sex-linked valvular dysplasia RGO:25093 RGO:25094 cerebellar hypoplasia, cavernous hemangioma, and coarctation of aorta RGO:25094 RGO:25097 diffuse capillary hemangiomas associated with localized skeletal hypotrophy RGO:25097 RGO:25098 Dirvy-van Bogaert syndrome RGO:25098 RGO:25099 disseminated hemangiomatosis RGO:25099 RGO:25100 facial hemangioma and dilation of carotid siphon RGO:25100 RGO:25102 familial cavernous malformations of central nervous system RGO:25102 RGO:25103 familial cavernous hemangioma RGO:25103 RGO:25104 familial cerebral arteriovenous malformations RGO:25104 RGO:25105 familial cerebral, hepatic, and retinal cavernous angiomas RGO:25105 RGO:25106 familial diffuse cystic angiomatosis of bone RGO:25106 RGO:25107 Servelle-Martorell syndrome RGO:25107 RGO:25108 pulmonary angiodysplasia RGO:25108 ORDO:90307 SNOMEDCT:234143003 RGO:25109 Parkes Weber syndrome RGO:25109 ORDO:1062 RGO:25110 hereditary neurocutaneous angioma RGO:25110 RGO:25111 hereditary cutaneous hemangiomas and spinal arteriovenous malformation RGO:25111 RGO:25112 hemangioma with right-sided aortic arch coarctation RGO:25112 tropical splenomegaly RGO:25116 tropical splenomegaly syndrome RGO:25116 SNOMEDCT:45256007 RGO:25117 Cruveilhier-Baumgarten syndrome RGO:25117 SNOMEDCT:79671001 RGO:25118 inferior vena cava syndrome RGO:25118 RGO:25120 idiopathic dilatation of thoracic systemic veins RGO:25120 RGO:25121 aneurysmal venous dilatation RGO:25121 RGO:25122 diverticulum of the superior vena cava RGO:25122 RGO:25123 Obui-Himo syndrome RGO:25123 ORDO:2834 SNOMEDCT:238875009 RGO:25124 wrinkly skin syndrome RGO:25124 ORDO:3455 SNOMEDCT:238874008 RGO:25125 Wiedemann-Rautenstrauch syndrome RGO:25125 RGO:25126 venous hemangiomatosis RGO:25126 RGO:25127 anomalous umbilical vein RGO:25127 RGO:25128 venous aneurysm with cystic hygroma RGO:25128 RGO:25129 iliocaval compression syndrome RGO:25129 iliac vein compression syndrome RADLEX:RID3307 SNOMEDCT:448804008 RGO:25130 May-Thurner syndrome RGO:25130 DOID:2988 ICD10CM:D68.61 SNOMEDCT:26843008 RGO:25134 antiphospholipid syndrome RGO:25134 RGO:25135 calcified inferior vena cava thrombus and adrenal hemorrhage RGO:25135 DOID:12169 HP:0012185 ICD10CM:G56.0 RADLEX:RID4647 SNOMEDCT:57406009 RGO:25136 carpal tunnel syndrome RGO:25136 RGO:25137 congenital renal vein thrombosis RGO:25137 RGO:25138 dextroposition with situs solitus RGO:25138 RGO:25139 bronchial artery dilatation RGO:25139 RGO:25140 peripheral arteriovenous malformations RGO:25140 RGO:25142 pulmonary laceration RGO:25142 SNOMEDCT:262784001 RGO:25143 pulmonary contusion RGO:25143 HP:0100845 ICD10CM:T78.2 SNOMEDCT:39579001 RGO:25146 anaphylaxis RGO:25146 RGO:25147 multi-system injury RGO:25147 RGO:25149 noxious fume inhalation RGO:25149 RGO:25150 paint inhalation RGO:25150 RGO:25151 cutaneous fistula RGO:25151 SNOMEDCT:89666000 RGO:25152 cardiopulmonary resuscitation RGO:25152 SNOMEDCT:182687005 RGO:25153 positive pressure ventilation RGO:25153 RGO:25154 sepsis with gas-forming organism RGO:25154 RGO:25157 metastatic Ewing sarcoma RGO:25157 RGO:25158 metastatic rhabdomyosarcoma RGO:25158 RGO:25159 metastatic Wilms tumor RGO:25159 RGO:25160 metastatic retinoblastoma RGO:25160 DOID:3384 SNOMEDCT:705145009 RGO:25161 metastatic osteosarcoma RGO:25161 RGO:25162 metastatic leukemia RGO:25162 ICD10CM:S22.2 SNOMEDCT:78516000 RGO:25163 fracture of sternum RGO:25163 SNOMEDCT:50448004 RGO:25164 fracture of spine RGO:25164 SNOMEDCT:33737001 RGO:25165 fracture of rib RGO:25165 RGO:25167 fibrous pseudotumor of pleura RGO:25167 SNOMEDCT:233758005 RGO:25168 mica pneumoconiosis RGO:25168 SNOMEDCT:51277007 RGO:25169 tin pneumoconiosis RGO:25169 DOID:10321 SNOMEDCT:50076003 RGO:25170 baritosis RGO:25170 SNOMEDCT:302450005 RGO:25171 talc pleurodesis RGO:25171 RGO:25172 infected pneumatocele RGO:25172 SNOMEDCT:471272001 RGO:25174 cavitary pneumonia RGO:25174 RGO:25175 traumatic lung cyst RGO:25175 RGO:25178 congenital orbital hypoplasia RGO:25178 HP:0004440 RGO:25179 coronal suture craniosynostosis RGO:25179 DOID:1361 RGO:25180 frontal sinus neoplasm RGO:25180 SNOMEDCT:39250009 RGO:25181 enucleation RGO:25181 RGO:25183 orbital dysplasia RGO:25183 DOID:6039 HP:0007716 ORDO:39044 RGO:25184 uveal melanoma RGO:25184 PHPV DOID:0060282 HP:0007968 ORDO:91495 SNOMEDCT:314270008 RGO:25185 persistent hyperplastic primary vitreous RGO:25185 RGO:25187 pseudoglioma RGO:25187 SNOMEDCT:128913004 SNOMEDCT:416864007 RGO:25188 retinocytoma RGO:25188 DOID:13025 ICD10CM:H35.1 ORDO:90050 RADLEX:RID3362 SNOMEDCT:415297005 RGO:25189 retinopathy of prematurity RGO:25189 HP:0007973 SNOMEDCT:95494009 RGO:25190 retinal dysplasia RGO:25190 DOID:9790 ICD10CM:B83.0 ORDO:3343 SNOMEDCT:406619001 RGO:25192 toxocariasis RGO:25192 DOID:184 RGO:25194 malignant bone neoplasm RGO:25194 DOID:3451 RGO:25195 skin carcinoma RGO:25195 RGO:25196 craniofacial malformation RGO:25196 RGO:25197 secondary orbital cellulitis RGO:25197 RGO:25198 secondary orbital abscess RGO:25198 DOID:10813 RGO:25199 nasal cavity lymphoma RGO:25199 RGO:25200 nasopharyngeal lymphoma RGO:25200 DOID:4931 RGO:25201 nasal cavity carcinoma RGO:25201 RGO:25202 primary bone tumor RGO:25202 RGO:25203 primary orbital neoplasm RGO:25203 DOID:3342 RADLEX:RID3524 SNOMEDCT:44462005 RGO:25205 osteitis RGO:25205 RGO:25206 congenital asymmetry RGO:25206 RGO:25207 congenital narrowing RGO:25207 RGO:25209 infratemporal chronic subdural hygroma RGO:25209 RGO:25210 temporal lobe astrocytoma RGO:25210 RGO:25211 infratemporal chronic subdural hematoma RGO:25211 SNOMEDCT:35386004 RGO:25212 superior orbital fissure syndrome RGO:25212 DOID:9310 RGO:25213 nasal cavity neoplasm RGO:25213 RGO:25214 anterior fossa neoplasm RGO:25214 RGO:25215 ophthalmic artery arteriovenous malformation RGO:25215 RGO:25216 ethmoid sinus carcinoma RGO:25216 RGO:25219 orbital infection RGO:25219 DOID:11234 SNOMEDCT:194005002 RGO:25220 orbital cellulitis RGO:25220 SNOMEDCT:39828002 RGO:25221 orbital abscess RGO:25221 RGO:25222 treated deprivation dwarfism RGO:25222 SNOMEDCT:387242007 SNOMEDCT:43684009 RGO:25223 misoprostol RGO:25223 RGO:25225 pseudo-achalasia RGO:25225 RGO:25226 esophageal leiomyomatosis RGO:25226 AFA HP:0009755 SNOMEDCT:400952003 RGO:25227 ankyloblepharon filiforme adnatum RGO:25227 MMT syndrome MODED syndrome ODED syndrome microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome microcephaly-oculo-digito-esophageal-duodenal syndrome oculo-digito-esophagoduodenal syndrome DOID:0060464 ORDO:1305 SNOMEDCT:702431004 RGO:25228 Feingold syndrome RGO:25228 RGO:25229 Mayer-Rokitansky syndrome RGO:25229 RGO:25230 congenital bile duct dilatation RGO:25230 ORDO:53693 SNOMEDCT:703388005 RGO:25231 GRACILE syndrome RGO:25231 RGO:25232 hepatic fibrosis-renal cystic disease RGO:25232 ORDO:99987 SNOMEDCT:698851003 RGO:25233 anophthalmia-esophageal-genital syndrome RGO:25233 SNOMEDCT:190444009 RGO:25234 hypogastrinemia RGO:25234 RGO:25236 otofacial syndrome RGO:25236 chloroma myeloid sarcoma DOID:8683 ICD10CM:C92.3 RADLEX:RID3857 SNOMEDCT:188738007 SNOMEDCT:35287006 RGO:25242 granulocytic sarcoma RGO:25242 RGO:25243 posttraumatic hemorrhage RGO:25243 RGO:25244 intratumoral hemorrhage RGO:25244 RGO:25245 posttraumatic hematoma RGO:25245 DOID:9740 ICD10CM:K91.5 SNOMEDCT:90782003 RGO:25246 postcholecystectomy syndrome RGO:25246 RGO:25247 colonic hyperganglionosis RGO:25247 RGO:25249 rectal myopathy RGO:25249 ORDO:158684 ORDO:79403 RGO:25251 epidermolysis bullosa-pyloric atresia complex RGO:25251 RGO:25253 intestinal neuronal dysplasia RGO:25253 HP:0000580 RGO:25258 pigmentary retinopathy RGO:25258 RGO:25259 Waugh syndrome RGO:25259 C. diff. colitis C. difficile C. difficile colitis Clostridium difficile pseudomembranous colitis DOID:0060185 RADLEX:RID3424 SNOMEDCT:423590009 RGO:25263 Clostridium difficile colitis RGO:25263 RGO:25264 Neurogenic megacolon RGO:25264 DOID:9258 ORDO:3440 SNOMEDCT:47434006 RGO:25265 Waardenburg syndrome RGO:25265 drug reaction with eosinophilia and systemic symptoms SNOMEDCT:702809001 RGO:25266 DRESS syndrome RGO:25266 ORDO:2604 SNOMEDCT:63684002 RGO:25269 familial visceral myopathy RGO:25269 pneumococcal endocarditis/meningitis/pneumonia RGO:25270 Austrian syndrome RGO:25270 RGO:25271 familial calcification of aorta and calcific aortic valve disease RGO:25271 Horten disease RGO:25272 giant cell aortitis RGO:25272 SNOMEDCT:47507006 RGO:25273 Rieger syndrome RGO:25273 DOID:0050644 RGO:25278 idiopathic infantile arterial calcification RGO:25278 RGO:25280 PC-1 NTPPPH deficiency RGO:25280 RGO:25284 partial trisomy 7 RGO:25284 RGO:25285 idiopathic dilatation of aorta RGO:25285 cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy hereditary multi-infarct dementia DOID:13945 ORDO:136 RADLEX:RID3360 RGO:25286 CADASIL RGO:25286 RGO:25287 familial supravalvular aortic stenosis and peripheral pulmonary stenosis RGO:25287 RGO:25291 brachysyndactyly RGO:25291 RGO:25292 acute aortic syndrome RGO:25292 SNOMEDCT:237602007 RGO:25295 insulin resistance syndrome RGO:25295 RGO:25297 hemodialysis access RGO:25297 RGO:25298 PHACE association RGO:25298 RGO:25299 anomalous origin of the right coronary artery from the pulmonary artery RGO:25299 RGO:25300 idiopathic multiple arterial stenoses RGO:25300 Bilginturan brachydactyly RGO:25301 Bilginturan syndrome RGO:25301 ORDO:221126 SNOMEDCT:700242002 RGO:25303 Fowler syndrome RGO:25303 fatal long QT syndrome HP:0001664 SNOMEDCT:31722008 RGO:25304 torsades de pointes RGO:25304 RGO:25307 ulnar deficiency RGO:25307 HP:0009777 RGO:25308 absent thumbs RGO:25308 RGO:25309 Sanchez-Cascos syndrome RGO:25309 HP:0001712 SNOMEDCT:55827005 RGO:25310 left ventricular hypertrophy RGO:25310 RGO:25315 malonic aciduria and malonyl CoA decarboxylase deficiency RGO:25315 ORDO:97238 SNOMEDCT:709281006 RGO:25316 rippling muscle disease RGO:25316 Tako-Tsubo syndrome Takotsubo cardiomyopathy Takotsubo syndrome ampulla cardiomyopathy apical ballooning syndrome ballooning cardiomyopathy transient left ventricular apical ballooning syndrome ORDO:66529 RGO:25317 Takotsubo-shaped cardiomyopathy RGO:25317 RGO:25318 Uruguay facio-cardio-musculo-skeletal syndrome RGO:25318 RGO:25321 cardiac conduction defect RGO:25321 RGO:25330 pugilist face RGO:25330 RGO:25331 muffled voice RGO:25331 RGO:25335 dense bones RGO:25335 HP:0001719 RGO:25336 double-outlet right ventricle RGO:25336 RGO:25337 Balci syndrome RGO:25337 RGO:25338 cardiomelic syndrome RGO:25338 RGO:25341 conotruncal-microphthalmia syndrome RGO:25341 faciocardiorenal syndrome RGO:25342 Eastman-Bixler syndrome RGO:25342 RGO:25343 familial hypertelorism RGO:25343 ORDO:1864 RGO:25344 familial sex-linked congenital valvular dysplasia RGO:25344 RGO:25348 ulnar agenesis RGO:25348 RGO:25349 duckbill lips RGO:25349 DOID:12270 HP:0000589 RGO:25350 coloboma RGO:25350 RGO:25351 ear defect RGO:25351 HP:0000077 RGO:25352 renal anomaly RGO:25352 DOID:13096 ORDO:820 SNOMEDCT:716745004 RGO:25353 Sneddon syndrome RGO:25353 DOID:0090127 RGO:25354 familial fibrosing serositis RGO:25354 RGO:25355 cutis marmorata-macrocephaly syndrome RGO:25355 RGO:25357 Urioste syndrome RGO:25357 RGO:25358 persistent Müllerian derivatives RGO:25358 RGO:25359 Njolstad syndrome RGO:25359 ORDO:2414 RGO:25360 congenital pulmonary lymphangiectasia RGO:25360 RGO:25361 limb lymphedema RGO:25361 RGO:25362 idiopathic pulmonary artery aneurysm RGO:25362 RGO:25363 balloon angioplasty complication RGO:25363 RGO:25364 familial platelet storage pool disease RGO:25364 SNOMEDCT:233944003 RGO:25365 familial primary pulmonary hypertension RGO:25365 RGO:25366 nevoid telangiectasia syndrome of pregnancy RGO:25366 RGO:25368 non-cirrhotic portal hypertension RGO:25368 hepatopulmonary syndrome SNOMEDCT:445237003 RGO:25369 portopulmonary hypertension RGO:25369 aortomesenteric left renal vein compression left renal vein entrapment syndrome renal nutcracker syndrome renal vein compression syndrome ORDO:71273 RADLEX:RID5294 RGO:25370 nutcracker syndrome RGO:25370 DOID:9346 SNOMEDCT:39402007 RGO:25371 pelvic congestion syndrome RGO:25371 RGO:25373 familial total anomalous pulmonary venous connection RGO:25373 RGO:25374 Paget-Schroetter syndrome RGO:25374 ORDO:2115 SNOMEDCT:716089008 RGO:25375 Harrod syndrome RGO:25375 RGO:25380 adenylyl cyclase dysfunction RGO:25380 RGO:25381 endocrine abnormality RGO:25381 HP:0200055 RGO:25383 small hands RGO:25383 HP:0001773 RGO:25384 small feet RGO:25384 RGO:25387 chromosome 9:del(9p) syndrome RGO:25387 RGO:25388 chromosome 14 uniparental disomy syndrome RGO:25388 RGO:25390 chromosome 15q dup syndrome RGO:25390 RGO:25391 chromosome 9q dup syndrome RGO:25391 SNOMEDCT:427207001 RGO:25393 abdominal compartment syndrome RGO:25393 DOID:0050471 ORDO:1359 RGO:25394 Carney complex RGO:25394 ORDO:314613 RGO:25395 growing teratoma syndrome RGO:25395 RGO:25397 littoral cell angioma of spleen RGO:25397 ORDO:314459 RGO:25398 pseudo-Meigs syndrome RGO:25398 ICD10CM:N99.83 SNOMEDCT:69911009 RGO:25399 residual ovary syndrome RGO:25399 RGO:25400 pelvic pain RGO:25400 HP:0030016 ICD10CM:N94.1 SNOMEDCT:71315007 RGO:25401 dyspareunia RGO:25401 DOID:5119 HP:0000138 RADLEX:RID34656 SNOMEDCT:79883001 RGO:25402 ovarian cyst RGO:25402 HP:0100615 SNOMEDCT:123843001 RGO:25403 ovarian tumor RGO:25403 SNOMEDCT:307340003 RGO:25404 monosomy 7 syndrome RGO:25404 DOID:0050438 ORDO:347 SNOMEDCT:445431000 RGO:25405 Frasier syndrome RGO:25405 ORDO:505 RGO:25406 Graham Little-Piccardi-Lassueur syndrome RGO:25406 DOID:161 SNOMEDCT:254666005 SNOMEDCT:26996000 RGO:25408 keratosis RGO:25408 SNOMEDCT:47757001 RGO:25409 corticosterone methyl oxidase type II deficiency RGO:25409 DOID:0080019 HP:0100255 ICD10CM:Q78.5 RGO:25411 metaphyseal dysplasia RGO:25411 RGO:25412 micropenis - congenital adrenal hypoplasia RGO:25412 DOID:53 HP:0011747 SNOMEDCT:399244003 RGO:25413 Pituitary disease RGO:25413 RGO:25414 hypoparathyroidism-retardation-dysmorphism RGO:25414 arthrogryposis-renal dysfunction-cholestasis syndrome DOID:0050763 RGO:25415 ARC syndrome RGO:25415 DOID:10632 ORDO:3463 SNOMEDCT:70694009 RGO:25416 Wolfram syndrome RGO:25416 ORDO:209905 RGO:25419 brain-thyroid-lung syndrome RGO:25419 DOID:12859 HP:0002072 SNOMEDCT:271700006 RGO:25420 chorea RGO:25420 DOID:12120 RADLEX:RID34650 SNOMEDCT:10501004 RGO:25421 pulmonary alveolar proteinosis RGO:25421 RGO:25422 endocrinopathy-ichthyosis syndrome RGO:25422 RGO:25423 postpartum autoimmune thyroid syndrome RGO:25423 RGO:25424 alopecia - ambiguous genitalia - laryngomalacia RGO:25424 RGO:25426 normal internal male genitalia RGO:25426 RGO:25427 external female genitalia RGO:25427 SNOMEDCT:42774007 RGO:25428 bilateral testes RGO:25428 ORDO:35107 SNOMEDCT:709490002 RGO:25429 desmosterolosis RGO:25429 RGO:25430 Kennerknecht syndrome RGO:25430 RGO:25431 methotrexate embryopathy RGO:25431 HP:0200024 RGO:25432 premature chromatid separation RGO:25432 RGO:25433 Sharony dysplasia RGO:25433 RGO:25437 short rib syndrome type 3 RGO:25437 HP:0004334 SNOMEDCT:400190005 RGO:25441 atrophic skin RGO:25441 DOID:1570 HP:0000656 SNOMEDCT:127559009 SNOMEDCT:62909004 RGO:25442 ectropion RGO:25442 RGO:25445 epimetaphyseal changes RGO:25445 HP:0002983 SNOMEDCT:74370006 RGO:25446 micromelia RGO:25446 DOID:0080173 ORDO:322 RGO:25447 exstrophy-epispadias complex RGO:25447 SNOMEDCT:95877004 RGO:25449 Gulf war syndrome RGO:25449 RGO:25451 valve bladder syndrome RGO:25451 ORDO:31043 RGO:25453 hypomagnesia-hypercalciuria-nephrocalcinosis syndrome RGO:25453 RGO:25456 fibuloulnar dysostosis-renal dysplasia RGO:25456 RGO:25458 ischiospinal dysostosis RGO:25458 RGO:25459 Wunderlich syndrome RGO:25459 RGO:25460 absent vertebral body ossification RGO:25460 RGO:25461 ribbon-like ribs RGO:25461 HP:0002664 RGO:25464 multiple neoplasia RGO:25464 RGO:25465 jaw ossifying fibroma RGO:25465 RGO:25466 renal hamartomas RGO:25466 RGO:25467 spontaneous renal hemorrhage RGO:25467 HP:0008660 ORDO:3033 SNOMEDCT:702397002 RGO:25468 renal tubular dysgenesis RGO:25468 DOID:2986 SNOMEDCT:236407003 RGO:25469 IgA glomerulonephritis RGO:25469 RGO:25472 Guadalajara camptodactyly type 3 RGO:25472 calvarial metastasis metastasis to the skull RGO:25475 skull metastasis RGO:25475 metastasis to the meninges RGO:25476 meningeal metastasis RGO:25476 childhood intracranial tumor RGO:25480 intracranial tumor in a child RGO:25480 SNOMEDCT:3750006 RGO:25482 arterial spasm RGO:25482 DOID:4193 HP:0005305 SNOMEDCT:71444005 RGO:25483 cerebral thrombosis RGO:25483 birth control pill contraceptive pill oral contraceptives SNOMEDCT:59261009 SNOMEDCT:5935008 RGO:25485 oral contraceptive RGO:25485 RADLEX:RID4825 SNOMEDCT:414086009 SNOMEDCT:55584005 RGO:25486 embolism RGO:25486 RGO:25496 nonglial brain neoplasm RGO:25496 RGO:25498 paraglioma RGO:25498 DOID:3078 ORDO:251589 RADLEX:RID4042 SNOMEDCT:55353007 RGO:25500 anaplastic astrocytoma RGO:25500 SNOMEDCT:115242003 RGO:25503 nerve sheath tumor RGO:25503 RGO:25504 nerve cell tumor RGO:25504 SNOMEDCT:277606000 RGO:25505 lymphoreticular tumor RGO:25505 Tumors of Maldevelopmental Origin RGO:25507 embryonal remnant tumor RGO:25507 RGO:25509 solitary intracranial mass RGO:25509 phakomatosis RADLEX:RID34753 SNOMEDCT:78572006 RGO:25510 neurocutaneous syndrome RGO:25510 RGO:25512 primary cerebral neuroblastoma RGO:25512 RGO:25522 basophilic adenoma RGO:25522 DOID:4916 HP:0011763 ORDO:300385 RADLEX:RID4255 SNOMEDCT:128665000 SNOMEDCT:254955001 RGO:25523 pituitary carcinoma RGO:25523 RGO:25524 eosinophilic adenoma RGO:25524 RGO:25526 external ear calcification RGO:25526 hearing loss HP:0000365 RGO:25527 deafness RGO:25527 HP:0008572 RGO:25528 external ear malformation RGO:25528 RGO:25529 advanced mastoid pneumatization RGO:25529 RGO:25530 underdeveloped mastoid RGO:25530 DOID:10348 HP:0000581 ICD10CM:H02.52 RGO:25535 blepharophimosis RGO:25535 HP:0000592 RGO:25536 blue sclerae RGO:25536 RGO:25537 intraorbital calcification RGO:25537 RGO:25538 cherry-red spot RGO:25538 DOID:6195 HP:0000509 ICD10CM:H10 SNOMEDCT:9826008 RGO:25539 conjunctivitis RGO:25539 HP:0000481 RGO:25540 corneal abnormality RGO:25540 HP:0001126 SNOMEDCT:400951005 RGO:25541 cryptophthalmos RGO:25541 HP:0000499 RGO:25542 abnormal eyelashes RGO:25542 RGO:25543 abnormal eyelid RGO:25543 decreased interorbital distance ocular hypotelorism orbital hypotelorism HP:0000601 SNOMEDCT:44593008 RGO:25545 hypotelorism RGO:25545 RGO:25546 abnormal iris RGO:25546 RGO:25547 abnormal lacrimal system RGO:25547 HP:0001083 RGO:25548 lens dislocation RGO:25548 HP:0000518 SNOMEDCT:193570009 RGO:25549 lens opacity RGO:25549 SNOMEDCT:93181004 RGO:25550 macrophthalmia RGO:25550 HP:0030961 SNOMEDCT:416671000 RGO:25551 microspherophakia RGO:25551 DOID:11830 HP:0000545 ICD10CM:H52.1 SNOMEDCT:57190000 RGO:25552 myopia RGO:25552 HP:0000639 ICD10CM:H55.0 SNOMEDCT:563001 RGO:25553 nystagmus RGO:25553 DOID:5723 HP:0000648 ICD10CM:H47.2 SNOMEDCT:76976005 RGO:25554 optic atrophy RGO:25554 RGO:25555 large orbit RGO:25555 RGO:25556 small orbit RGO:25556 DOID:146 HP:0001085 ICD10CM:H47.1 SNOMEDCT:423341008 RGO:25557 papilledema RGO:25557 HP:0000508 RGO:25558 eyelid ptosis RGO:25558 HP:0000488 SNOMEDCT:29555009 RGO:25559 retinopathy RGO:25559 RGO:25561 eyebrow anomaly RGO:25561 SNOMEDCT:78113001 RGO:25562 cherubic facies RGO:25562 HP:0000274 RGO:25563 facial hypoplasia RGO:25563 RGO:25564 antegonial notching of the mandible RGO:25564 RGO:25565 mandibular agenesis/dysgenesis RGO:25565 HP:0000202 RGO:25566 cleft lip/palate RGO:25566 RGO:25567 lip defect RGO:25567 HP:0000171 ICD10CM:Q38.3 SNOMEDCT:32614006 RGO:25568 microglossia RGO:25568 HP:0000160 ICD10CM:Q18.5 SNOMEDCT:14582003 RGO:25569 microstomia RGO:25569 RGO:25570 salivary gland/duct abnormality RGO:25570 DOID:9637 HP:0010280 SNOMEDCT:61170000 RGO:25571 stomatitis RGO:25571 HP:0000157 RGO:25572 tongue abnormality RGO:25572 HP:0011803 ORDO:2695 RGO:25574 bifid nose RGO:25574 flat nasal bridge HP:0005280 RGO:25575 depressed nasal bridge RGO:25575 HP:0100582 SNOMEDCT:52756005 RGO:25576 nasal polyposis RGO:25576 HP:0000414 RGO:25577 bulbous nose RGO:25577 HP:0003196 SNOMEDCT:249310005 RGO:25578 small nose RGO:25578 Kleeblattschädel Kleeblattschädel anomaly cloverleaf skull triphyllocephaly HP:0002676 RGO:25579 cloverleaf skull deformity RGO:25579 delayed closure of fontanelle HP:0000239 SNOMEDCT:276709006 RGO:25580 large fontanelle RGO:25580 HP:0002700 RGO:25581 large foramen magnum RGO:25581 HP:0002677 RGO:25582 small foramen magnum RGO:25582 macrocrania megalencephaly DOID:2186 HP:0000256 ICD10CM:Q75.3 SNOMEDCT:19410003 RGO:25583 macrocephaly RGO:25583 HP:0002690 RGO:25584 large sella turcica RGO:25584 HP:0010538 RGO:25585 small sella turcica RGO:25585 RGO:25586 acquired skull defect RGO:25586 HP:0002678 RGO:25587 skull asymmetry RGO:25587 RGO:25588 congenital skull defect RGO:25588 hair-on-end pattern in skull RADLEX:RID35253 RGO:25589 hair-on-end skull RGO:25589 skull hyperostosis HP:0004490 RGO:25590 calvarial hyperostosis RGO:25590 SNOMEDCT:248380007 RGO:25591 thick skull RGO:25591 RGO:25592 wide sutures RGO:25592 multiple sutural bones sutural bones HP:0002645 SNOMEDCT:113194005 RGO:25593 Wormian bones RGO:25593 RGO:25594 anodontia or hypodontia RGO:25594 SNOMEDCT:89988002 RGO:25595 dental cyst RGO:25595 RGO:25596 dental defect RGO:25596 HP:0000695 SNOMEDCT:21995002 RGO:25597 natal teeth RGO:25597 HP:0006315 RGO:25598 single maxillary central incisor RGO:25598 HP:0000679 ICD10CM:K00.2 ORDO:3289 SNOMEDCT:51744007 RGO:25599 taurodontism RGO:25599 RGO:25601 floating teeth RGO:25601 HP:0006480 SNOMEDCT:42756003 RGO:25602 premature tooth loss RGO:25602 RGO:25603 diaphragm dysfunction RGO:25603 muscular hypertrophy RGO:25604 muscle enlargement RGO:25604 DOID:767 HP:0003202 SNOMEDCT:88092000 RGO:25605 muscular atrophy RGO:25605 SNOMEDCT:193237003 RGO:25606 myotonic disorder RGO:25606 RGO:25607 pectoral muscle deficiency RGO:25607 RGO:25608 branchial arch anomaly RGO:25608 HP:0002135 RGO:25612 basal ganglion calcification RGO:25612 RGO:25613 cerebral gyriform calcification RGO:25613 HP:0002514 RGO:25614 intracranial calcification RGO:25614 RGO:25615 cerebellar dysgenesis RGO:25615 RGO:25616 cerebrovascular malformation RGO:25616 RGO:25617 agenesis or hypoplasia of the corpus callosum RGO:25617 RGO:25619 cranial nerve paresis or paralysis RGO:25619 RGO:25620 encephalocele/meningocele RGO:25620 HP:0007206 ORDO:99802 SNOMEDCT:253170008 RGO:25621 hemimegalencephaly RGO:25621 RGO:25622 hypothalamic hamartoblastoma syndrome RGO:25622 RGO:25623 leukodystrophy / leukoencephalopathy RGO:25623 RGO:25625 abnormal septum pellucidum RGO:25625 RGO:25627 bowed tubular bones RGO:25627 DOID:0050581 HP:0001156 SNOMEDCT:43476002 RGO:25628 brachydactyly RGO:25628 RGO:25630 multiple calcaneal ossification centers RGO:25630 HP:0030084 SNOMEDCT:17268007 RGO:25632 clinodactyly RGO:25632 club foot talipes equinovarus DOID:11836 HP:0001762 SNOMEDCT:397932003 RGO:25633 clubfoot RGO:25633 cortical hyperostosis RGO:25634 cortical bone thickening RGO:25634 epiphyseal bracket longitudinally bracketed epiphysis RGO:25635 delta phalanx RGO:25635 digital absence RGO:25636 absent digit RGO:25636 RGO:25637 dumbbell-shaped tubular bones RGO:25637 RGO:25638 bone duplication RGO:25638 HP:0000943 SNOMEDCT:254069004 RGO:25639 dysostosis multiplex RGO:25639 HP:0100257 SNOMEDCT:81208006 RGO:25640 ectrodactyly RGO:25640 HP:0003042 RGO:25641 elbow dislocation RGO:25641 ball-in-socket deformity coned epiphysis HP:0010579 RGO:25642 cone-shaped epiphysis RGO:25642 megaepiphysis RGO:25644 large epiphysis RGO:25644 RGO:25645 epiphyseal necrosis RGO:25645 RGO:25646 premature epiphyseal fusion RGO:25646 RGO:25648 ring-shaped epiphysis RGO:25648 RGO:25649 small epiphysis RGO:25649 RADLEX:RID34412 RGO:25650 Erlenmeyer flask deformity RGO:25650 RGO:25651 early femoral head ossification RGO:25651 SCFE slipped femoral head RADLEX:RID4781 RGO:25653 slipped capital femoral epiphysis RGO:25653 HP:0002980 RGO:25654 bowed femur RGO:25654 PFFD hypoplasia of proximal femur proximal femoral focal deficiency RGO:25655 proximal femoral deficiency RGO:25655 RGO:25656 abnormal fibula RGO:25656 knock-knee knock-knees HP:0002857 ICD10CM:M21.06 RGO:25657 genu valgum RGO:25657 bowleg bowlegs HP:0002970 ICD10CM:M21.16 RGO:25658 genu varum RGO:25658 HP:0030043 RGO:25661 hip subluxation RGO:25661 accessory phalanges accessory phalanx RGO:25662 hyperphalangism RGO:25662 RGO:25663 degenerative joint changes RGO:25663 RGO:25664 joint subluxation RGO:25664 joint hypermobility HP:0001388 SNOMEDCT:298203008 RGO:25665 joint laxity RGO:25665 joint contracture HP:0001376 RGO:25666 limited joint mobility RGO:25666 RGO:25667 limb overgrowth RGO:25667 RGO:25668 limb reduction RGO:25668 HP:0003067 ORDO:35688 RADLEX:RID35359 SNOMEDCT:4530000 RGO:25670 Madelung deformity RGO:25670 RGO:25671 bone medullary space stenosis RGO:25671 RGO:25672 mesomelic limb shortness RGO:25672 HP:0010034 RGO:25673 short first metacarpal RGO:25673 HP:0010049 RGO:25674 short metacarpal RGO:25674 broad metaphysis flared metaphysis flaring of the metaphyses splaying of the metaphyses wide metaphyses RGO:25677 wide metaphysis RGO:25677 HP:0010743 RGO:25678 short metatarsals RGO:25678 abnormal patella RGO:25679 malformed patella RGO:25679 RGO:25680 periosteal cloaking RGO:25680 DOID:1148 HP:0010442 ICD10CM:Q69 SNOMEDCT:367506006 RGO:25682 polydactyly RGO:25682 radial-side polydactyly HP:0100258 SNOMEDCT:205135003 RGO:25683 preaxial polydactyly RGO:25683 HP:0002984 RGO:25684 radial ray hypoplasia RGO:25684 RGO:25685 rhizomelic limb shortness RGO:25685 RGO:25686 slender tubular long bones RGO:25686 RGO:25687 longitudinal metaphyseal-diaphyseal striations RGO:25687 RGO:25688 humerus-radius-ulna synostosis RGO:25688 RGO:25689 tubular bone synostosis RGO:25689 TPT HP:0001199 ICD10CM:Q74.0 SNOMEDCT:205308004 RGO:25692 triphalangeal thumb RGO:25692 HP:0001837 RGO:25694 broad toe RGO:25694 RGO:25695 ulnar ray hypoplasia RGO:25695 RGO:25696 vertical talus RGO:25696 flared iliac wing RGO:25697 small acetabular angle RGO:25697 iliac crest serration lacy pelvis RGO:25698 serrated iliac crest RGO:25698 hypoplastic ilia hypoplastic ilium small pelvis HP:0008839 RGO:25699 hypoplastic pelvis RGO:25699 small sacroiliac notches small sciatic notches RGO:25702 small sciatic notch RGO:25702 RGO:25703 disk calcification RGO:25703 RGO:25705 presacral mass RGO:25705 decreased interpedicular distance HP:0003416 RGO:25706 narrow spinal canal RGO:25706 increased interpedicular distance RGO:25707 wide spinal canal RGO:25707 RGO:25709 minimal vertebral ossification RGO:25709 RGO:25710 vertebral anomaly RGO:25710 RGO:25711 anterior beaked vertebral body RGO:25711 RGO:25712 vertebral coronal cleft RGO:25712 vertebral segmentation defect RGO:25713 vertebral malsegmentation RGO:25713 RGO:25714 tall vertebrae RGO:25714 RGO:25717 resorption of distal clavicle RGO:25717 lateral hook of clavicle HP:0000895 SNOMEDCT:249684000 RGO:25718 hooked clavicle RGO:25718 RGO:25719 slender clavicle RGO:25719 RGO:25720 shallow glenoid fossa RGO:25720 RGO:25721 rib anomaly RGO:25721 RGO:25722 beaded rib RGO:25722 11 pairs of ribs RGO:25723 decreased number of ribs RGO:25723 rib flaring RGO:25724 flaring of ribs RGO:25724 HP:0030280 RGO:25725 rib gap RGO:25725 rib erosion RGO:25726 rib notching RGO:25726 HP:0000773 RGO:25727 short ribs RGO:25727 13 or more ribs RGO:25729 supernumerary rib RGO:25729 thickened ribs wide ribs RGO:25730 thick ribs RGO:25730 RGO:25731 abnormal scapula RGO:25731 RGO:25732 abnormal sternum RGO:25732 HP:0006644 RGO:25733 thoracic dysplasia RGO:25733 DOID:381 HP:0003040 RADLEX:RID5393 SNOMEDCT:399269003 RGO:25734 arthropathy RGO:25734 generalized accelerated skeletal maturation increased bone age HP:0005616 SNOMEDCT:123982003 RGO:25736 advanced bone age RGO:25736 RGO:25737 advanced bone age in a newborn RGO:25737 generalized retarded skeletal maturation HP:0002750 SNOMEDCT:123983008 RGO:25738 delayed bone age RGO:25738 SNOMEDCT:302861008 SNOMEDCT:83944004 RGO:25740 chondromatosis RGO:25740 RGO:25741 craniotubular dysplasia RGO:25741 DOID:204 RADLEX:RID5073 SNOMEDCT:23680005 RGO:25742 enthesopathy RGO:25742 DOID:203 ICD10CM:M27.8 SNOMEDCT:416189003 SNOMEDCT:80400009 RGO:25743 exostosis RGO:25743 HP:0002756 RADLEX:RID4683 SNOMEDCT:22640007 RGO:25744 pathologic fracture RGO:25744 hemihyperplasia HP:0001528 ORDO:2128 RGO:25745 hemihypertrophy RGO:25745 HP:0005716 RGO:25746 lethal skeletal dysplasia RGO:25746 RGO:25747 lytic skeletal lesion RGO:25747 DOID:4254 HP:0011001 RADLEX:RID5228 SNOMEDCT:49347007 RGO:25748 osteosclerosis RGO:25748 hypotrichosis sparse hair DOID:987 HP:0001596 SNOMEDCT:56317004 RGO:25751 alopecia RGO:25751 café-au-lait patches HP:0000957 SNOMEDCT:201281002 RGO:25753 café-au-lait spots RGO:25753 DOID:2723 HP:0000964 SNOMEDCT:43116000 RGO:25754 eczema RGO:25754 HP:0002299 SNOMEDCT:25159003 RGO:25755 brittle hair RGO:25755 RGO:25756 hair color abnormality RGO:25756 RGO:25758 low hairline RGO:25758 HP:0000975 SNOMEDCT:312230002 RGO:25759 hyperhidrosis RGO:25759 HP:0000962 RADLEX:RID3786 SNOMEDCT:26996000 SNOMEDCT:396228006 RGO:25760 hyperkeratosis RGO:25760 hypertrichosis HP:0001007 ICD10CM:L68.0 SNOMEDCT:399939002 RGO:25761 hirsutism RGO:25761 fish skin ichthyosiform dermatosis ichthyosiform lesion thick skin DOID:1697 HP:0008064 SNOMEDCT:13059002 RGO:25762 ichthyosis RGO:25762 SNOMEDCT:89077005 RGO:25764 nail discoloration RGO:25764 HP:0001806 ICD10CM:L60.1 SNOMEDCT:75789001 RGO:25765 onycholysis RGO:25765 HP:0007618 RADLEX:RID34252 RGO:25767 skin calcification RGO:25767 SNOMEDCT:301854006 RGO:25768 skin dimple RGO:25768 HP:0000988 SNOMEDCT:271807003 RGO:25769 skin rash RGO:25769 HP:0000992 RGO:25771 skin photosensitivity RGO:25771 RGO:25772 skin pigment abnormality RGO:25772 acrochordon DOID:6873 SNOMEDCT:201091002 SNOMEDCT:31069005 RGO:25773 skin tag RGO:25773 HP:0100678 SNOMEDCT:247434009 RGO:25774 wrinkled skin RGO:25774 RGO:25775 basal cell carcinoma in children RGO:25775 DOID:3165 RGO:25776 skin neoplasm RGO:25776 RGO:25777 familial neoplasm RGO:25777 RGO:25778 fibrous tumor RGO:25778 DOID:255 HP:0001028 ICD10CM:D18.0 RADLEX:RID3969 SNOMEDCT:2099007 SNOMEDCT:400210000 RGO:25779 hemangioma RGO:25779 DOID:14566 HP:0002664 RGO:25780 increased risk of neoplasm RGO:25780 absence of adipose tissue adipose tissue deficiency HP:0100578 SNOMEDCT:248315005 RGO:25782 lipoatrophy RGO:25782 RGO:25783 body asymmetry RGO:25783 RGO:25784 breast abnormality RGO:25784 RGO:25785 fingertip calcification RGO:25785 RGO:25786 soft-tissue calcification RGO:25786 generalized overgrowth or elongation of the skeleton giantism macrosomia DOID:2446 ORDO:99725 SNOMEDCT:80849007 RGO:25787 gigantism RGO:25787 DOID:12698 HP:0000771 ICD10CM:N62 RADLEX:RID34665 SNOMEDCT:4754008 RGO:25788 gynecomastia RGO:25788 hamartoma syndrome SNOMEDCT:399960008 RGO:25789 hamartomatosis RGO:25789 DOID:1097 HP:0001789 ORDO:1041 RADLEX:RID39322 SNOMEDCT:276508000 RGO:25792 hydrops fetalis RGO:25792 RGO:25793 immune disorder RGO:25793 RGO:25794 marfanoid appearance RGO:25794 RGO:25795 mitochondrial disorder RGO:25795 RGO:25796 nipple anomaly RGO:25796 RGO:25797 soft-tissue ossification RGO:25797 RGO:25798 predominantly ectodermal phakomatosis RGO:25798 RGO:25799 predominantly endodermal phakomatosis RGO:25799 RGO:25800 predominantly mesodermal phakomatosis RGO:25800 progeroid appearance SNOMEDCT:88587007 RGO:25801 premature aging RGO:25801 RADLEX:RID34686 SNOMEDCT:87628006 RGO:25804 bacterial infection RGO:25804 ORDO:1458 RGO:25806 CODAS syndrome RGO:25806 RGO:25807 hereditary external ear ossification RGO:25807 RGO:25808 idiopathic calcification of the auricular cartilage RGO:25808 RGO:25809 progressive muscular wasting - unusual facies - cataracts - mental deficiency - ossification of pinnae - generalized osteoporosis RGO:25809 RGO:25810 solitary congenital nodular calcification of Winer RGO:25810 ORDO:998 RGO:25812 X-linked albinism and deafness RGO:25812 RGO:25816 autosomal dominant hearing loss RGO:25816 RGO:25817 Barrter syndrome RGO:25817 DOID:0050677 ORDO:123 RGO:25820 Bjornstad syndrome RGO:25820 DOID:0050678 ICD10CM:M04.8 ORDO:90340 SNOMEDCT:699861000 RGO:25821 Blau syndrome RGO:25821 RGO:25823 brachydactyly-mental retardation-deafness RGO:25823 RGO:25824 branchio-oto-costal syndrome RGO:25824 RGO:25825 branchiootorenal dysplasia syndrome RGO:25825 RGO:25831 cataracts - radiculomegaly - septal defect - deafness RGO:25831 cataracts DOID:83 HP:0000518 SNOMEDCT:128306009 SNOMEDCT:193570009 RGO:25832 cataract RGO:25832 DOID:0050753 HP:0001251 SNOMEDCT:85102008 RGO:25833 cerebellar ataxia RGO:25833 DOID:10595 ICD10CM:G60.0 RADLEX:RID34634 RGO:25834 Charcot-Marie-Tooth disease RGO:25834 ORDO:314597 RGO:25838 Chudley-McCullough syndrome RGO:25838 RGO:25841 craniodiaphysial dysplasia RGO:25841 RGO:25850 MIDD syndrome RGO:25850 DOID:693 HP:0006297 RGO:25855 dental enamel hypoplasia RGO:25855 RGO:25860 CHARGE-like syndrome RGO:25860 RGO:25862 familial osteochondrodysplastic dwarfism RGO:25862 RGO:25863 FAOR syndrome RGO:25863 RGO:25864 fetal rubella infection RGO:25864 ORDO:1272 RGO:25865 Fine-Lubinsky syndrome RGO:25865 ORDO:3219 RGO:25867 Fountain syndrome RGO:25867 RGO:25868 Groll-Hirschowitz syndrome RGO:25868 Barakat syndrome DOID:0060878 RGO:25870 HDR syndrome RGO:25870 RGO:25871 juvenile hypothyroidism RGO:25871 ORDO:90647 SNOMEDCT:373905003 RGO:25873 Jervell and Lange-Nielsen syndrome RGO:25873 ORDO:93972 RGO:25875 Juberg-Marsidi syndrome RGO:25875 Bernardinelli-Seip syndrome congenital total lipodystrophy lipoatrophic diabetes lipoid diabetes DOID:811 HP:0009125 SNOMEDCT:71325002 RGO:25883 lipodystrophy RGO:25883 metaphyseal dysplasia Jansen type ORDO:33067 RGO:25887 metaphyseal chondrodysplasia Jansen type RGO:25887 ORDO:2502 RGO:25889 metaphyseal dysostosis-deafness RGO:25889 RGO:25890 Michel aplasia/dysplasia RGO:25890 RGO:25891 microtia-cardiac defect-deafness RGO:25891 DOID:11502 HP:0001653 RADLEX:RID34748 SNOMEDCT:48724000 RGO:25892 mitral valve insufficiency RGO:25892 deafness-dystonia syndrome DOID:0050757 ORDO:52368 SNOMEDCT:702423009 RGO:25893 Mohr-Tranebjaerg syndrome RGO:25893 HP:0000376 RGO:25894 Mondini malformation RGO:25894 ORDO:585 SNOMEDCT:54898003 RGO:25897 multiple sulfatase deficiency RGO:25897 RGO:25898 myopia - corneal dystrophy - deafness RGO:25898 OSMED oto-spondylo-megaepiphyseal dysplasia DOID:0080026 ORDO:1427 SNOMEDCT:254060000 RGO:25913 otospondylomegaepiphyseal dysplasia RGO:25913 ORDO:2791 RGO:25914 otodental dysplasia RGO:25914 ORDO:2202 RGO:25916 palmoplantar hyperkeratosis and deafness RGO:25916 DOID:0050857 ORDO:2855 SNOMEDCT:93466004 RGO:25917 Perrault syndrome RGO:25917 RGO:25921 radial ray aplasia RGO:25921 RGO:25922 Rasmussen syndrome type 2 RGO:25922 RGO:25923 Renal-genital-ear anomalies RGO:25923 RGO:25924 Richieri-Costa syndrome RGO:25924 RGO:25927 Sebastian syndrome RGO:25927 DOID:0050439 ORDO:886 SNOMEDCT:57838006 RGO:25939 Usher syndrome RGO:25939 RGO:25940 vascular-facial dysmorphism syndrome RGO:25940 RGO:25941 Vohwinkel syndrome RGO:25941 DOID:0050566 RGO:25943 X-linked deafness RGO:25943 RGO:25944 X-linked sensorineural deafness RGO:25944 RGO:25946 absent ear lobe RGO:25946 RGO:25948 aminopterin-fetopathy-like syndrome RGO:25948 DOID:12271 HP:0000526 ICD10CM:Q13.1 ORDO:77 SNOMEDCT:69278003 RGO:25949 aniridia RGO:25949 HP:0000413 RGO:25950 auditory canal atresia RGO:25950 RGO:25952 aural exostosis RGO:25952 ORDO:137888 RGO:25953 auricular-condylar syndrome RGO:25953 RGO:25954 auriculoosteodysplasia syndrome RGO:25954 DOID:0050691 SNOMEDCT:449821007 RGO:25956 branchiooculofacial syndrome RGO:25956 RGO:25959 cleft ear lobe RGO:25959 DOID:0080033 ORDO:1522 SNOMEDCT:36601008 RGO:25962 craniometaphyseal dysplasia RGO:25962 HP:0000378 RGO:25964 cupped ear RGO:25964 tubercle of helix in midsegment SNOMEDCT:29715005 RGO:25965 Darwin tubercle RGO:25965 RGO:25966 ear lobe pit/sinus RGO:25966 RGO:25967 ectopic pinna RGO:25967 RGO:25968 exchondrosis of pinna RGO:25968 SNOMEDCT:89000008 RGO:25972 hypertrichosis pinnae auris RGO:25972 RGO:25973 hypertrophic ear lobe RGO:25973 HP:0000394 SNOMEDCT:76223006 RGO:25978 lop ear RGO:25978 HP:0008551 ICD10CM:Q17.2 ORDO:83463 SNOMEDCT:35045004 RGO:25981 microtia RGO:25981 Moebius syndrome DOID:13501 RGO:25982 Möbius syndrome RGO:25982 bulging superior margin of pinna with fused crura of the anthelix and the crus helicis HP:0030677 RGO:25983 Mozart ear RGO:25983 RGO:25984 oto-facial syndrome plus RGO:25984 RGO:25985 oto-onychoperoneal syndrome RGO:25985 HP:0100687 ICD10CM:Q17.0 SNOMEDCT:35547002 RGO:25986 polyotia RGO:25986 ORDO:246 SNOMEDCT:66038001 RGO:25987 postaxial acrofacial dysostosis syndrome RGO:25987 RGO:25988 renal-genital-ear anomaly RGO:25988 ORDO:2077 RGO:25998 German syndrome RGO:25998 RGO:26002 Pfeiffer type cardiocranial syndrome RGO:26002 3C syndrome CCC dysplasia craniocerebellocardiac dysplasia RGO:26003 Ritscher-Shinzel syndrome RGO:26003 DOID:11337 ORDO:137839 RGO:26011 Lemierre syndrome RGO:26011 RGO:26013 joint hyperlaxity RGO:26013 HP:0001999 SNOMEDCT:248200007 RGO:26014 dysmorphic facies RGO:26014 RGO:26015 ear canal malformation RGO:26015 RGO:26016 hypoplastic toenail RGO:26016 HP:0005872 RGO:26017 brachytelomesophalangy RGO:26017 RGO:26018 bilateral cryptomincrotia RGO:26018 HP:0000400 RGO:26020 large ears RGO:26020 RGO:26022 ectodermal defect RGO:26022 RGO:26025 partial aplasia of the nails RGO:26025 RGO:26026 aplasia of the fibula RGO:26026 RGO:26027 hypoplasia of the fibula RGO:26027 ICD10CM:Q17.0 SNOMEDCT:35547002 RGO:26028 accessory auricle RGO:26028 RGO:26030 hypoplasia of the nipple RGO:26030 RGO:26032 midline defect RGO:26032 HP:0000972 RGO:26035 palmoplantar hyperkeratosis RGO:26035 ICD10CM:M72.1 SNOMEDCT:16687001 RGO:26036 knuckle pads RGO:26036 HP:0001820 SNOMEDCT:111202002 RGO:26037 leukonychia RGO:26037 RGO:26040 motion disorder RGO:26040 HP:0005736 RGO:26042 hypoplasia of the tibia RGO:26042 HP:0009795 SNOMEDCT:204268008 RGO:26043 branchial fistula RGO:26043 RGO:26045 ear pits RGO:26045 HP:0100267 RGO:26046 lip pit RGO:26046 RGO:26047 brain anomaly RGO:26047 RGO:26048 kidney dysplasia RGO:26048 RGO:26050 pontobulbar palsy RGO:26050 HP:0001274 SNOMEDCT:5102002 RGO:26052 absent corpus callosum RGO:26052 RGO:26055 premature senility RGO:26055 RGO:26056 cutaneous atrophy RGO:26056 RGO:26058 chronic recurrent urticaria RGO:26058 RGO:26059 periodic arthritis RGO:26059 ORDO:85445 SNOMEDCT:281034005 RGO:26062 secondary amyloidosis RGO:26062 HP:0004409 SNOMEDCT:83156004 RGO:26064 hyposmia RGO:26064 HP:0000405 SNOMEDCT:44057004 RGO:26065 conductive deafness RGO:26065 HP:0000458 ICD10CM:R43.0 RADLEX:RID28792 SNOMEDCT:44169009 RGO:26066 anosmia RGO:26066 HP:0001510 RGO:26067 growth failure RGO:26067 HP:0000405 SNOMEDCT:44057004 RGO:26069 conductive hearing loss RGO:26069 HP:0008873 RGO:26070 short-limbed dwarfism RGO:26070 DOID:1432 HP:0000618 RGO:26072 blindness RGO:26072 DOID:1307 HP:0000726 RADLEX:RID5136 SNOMEDCT:52448006 RGO:26073 dementia RGO:26073 RGO:26076 dental hypoplasia RGO:26076 RGO:26079 synechiae RGO:26079 SNOMEDCT:95709007 RGO:26080 atrophy of iris RGO:26080 flexion deformity of one or more digits HP:0012385 SNOMEDCT:29271008 RGO:26083 camptodactyly RGO:26083 RGO:26084 wasting of hand muscles RGO:26084 SNOMEDCT:205683001 RGO:26085 ovarian dysgenesis RGO:26085 DOID:1699 SNOMEDCT:268282005 RGO:26089 ichthyosiform erythroderma RGO:26089 DOID:10003 HP:0000407 SNOMEDCT:60700002 RGO:26090 sensorineural deafness RGO:26090 RGO:26091 vascularized cornea RGO:26091 RGO:26092 cerebral microangiopathy RGO:26092 RGO:26093 retinal microangiopathy RGO:26093 HP:0001762 RGO:26094 club feet RGO:26094 DOID:4677 HP:0000491 ICD10CM:H16 SNOMEDCT:5888003 RGO:26095 keratitis RGO:26095 RGO:26097 dental anomaly RGO:26097 RGO:26099 Escher-Hirt syndrome RGO:26099 DOID:14702 RGO:26106 branchiootorenal dysplasia RGO:26106 Patau syndrome DOID:11665 ORDO:3378 RGO:26107 trisomy 13 RGO:26107 RGO:26109 congenital aplasia of semicircular canals RGO:26109 EVA syndrome EVAS enlarged vestibular aqueduct syndrome RGO:26110 endolymphatic duct/sac syndrome RGO:26110 hypertelorism-microtia-clefting syndrome DOID:14670 ORDO:2213 RGO:26111 hypertelorism-microtia-facial clefting syndrome RGO:26111 RGO:26113 Mondini dysplasia RGO:26113 RGO:26116 Rieger syndrome-plus RGO:26116 RGO:26117 Schnizel-Giedion syndrome RGO:26117 RGO:26119 atypical osteopetrosis and posterior helical ear pits RGO:26119 RGO:26120 Burn-McKeown syndrome RGO:26120 RGO:26121 da Silva syndrome RGO:26121 RGO:26123 Delleman syndrome RGO:26123 RGO:26124 familial posterior helical ear pits RGO:26124 RGO:26129 renal tubular dysgenesis-absent nipples syndrome RGO:26129 ankyloblepharon-ectodermal dysplasia-cleft lip/palate SNOMEDCT:55821006 RGO:26130 ankyloblepharon-ectodermal dysplasia-clefting syndrome RGO:26130 RGO:26131 ankyloblepharon-ectrodactyly syndrome RGO:26131 autosomal recessive popliteal pterygium syndrome lethal popliteal pterygium syndrome ORDO:1234 RGO:26132 Bartsocas-Papas syndrome RGO:26132 RGO:26134 acrocallosal-like syndrome RGO:26134 RGO:26140 anophthalmia-hypothalamic disorder RGO:26140 RGO:26141 anophthalmia-absent pituitary-nephronophthisis-dysmorphology RGO:26141 ORDO:1104 RGO:26142 anophthalmia-plus syndrome RGO:26142 ORDO:66625 RGO:26144 cerebro-oculo-nasal syndrome RGO:26144 RGO:26145 chondrodysplasia-microphthalmia RGO:26145 ORDO:93267 RGO:26148 cloverleaf skull-MCA-dysplasia RGO:26148 ORDO:98938 SNOMEDCT:715771008 RGO:26149 colobomatous microphthalmia RGO:26149 Cross-McKusick-Breen syndrome hypopigmentation and microphthalmia oculocerebral-hypopigmentation syndrome ICD10CM:E70.328 ORDO:2719 SNOMEDCT:17827007 RGO:26150 Cross syndrome RGO:26150 RGO:26154 familial microphthalmos RGO:26154 DOID:0050819 ORDO:2470 RGO:26156 Matthew-Wood syndrome RGO:26156 RGO:26158 maternal medication abuse RGO:26158 RGO:26159 Michelin tire baby-like syndrome RGO:26159 RGO:26165 microphthalmia-cyst-medulloblastoma syndrome RGO:26165 RGO:26166 microphthalmos-hypothalamic disorder RGO:26166 RGO:26168 MIDAS syndrome RGO:26168 DOID:0060599 ORDO:627 SNOMEDCT:445257004 RGO:26169 Nance-Horan syndrome RGO:26169 ORDO:2712 SNOMEDCT:699300009 RGO:26170 oculofaciocardiodental syndrome RGO:26170 ORDO:2714 RGO:26171 oculo-palato-cerebral syndrome RGO:26171 SNOMEDCT:703403003 RGO:26172 ophthalmo-acromelic syndrome RGO:26172 ORDO:2763 RGO:26173 osteocraniostenosis RGO:26173 RGO:26174 pulmonary agenesis-diaphragmatic hernia-microphthalmia syndrome RGO:26174 DOID:12117 ICD10CM:J84.02 ORDO:60025 RADLEX:RID34608 SNOMEDCT:87153008 RGO:26175 pulmonary alveolar microlithiasis RGO:26175 RGO:26176 Sakoda complex RGO:26176 DOID:9258 ORDO:897 RGO:26177 Shah-Waardenburg syndrome RGO:26177 DOID:0060861 SNOMEDCT:703403003 RGO:26179 Waardenburg anophthalmia syndrome RGO:26179 RGO:26181 Arnold-Chiari-syringomyelia syndrome RGO:26181 RGO:26182 blepharofacioskeletal syndrome RGO:26182 RGO:26183 blepharo-naso-facial syndrome RGO:26183 SNOMEDCT:79833006 RGO:26184 familial blepharophimosis syndrome RGO:26184 ORDO:126 RGO:26189 blepharophimosis-ptosis-epicanthus inversus syndrome RGO:26189 RGO:26193 frontofacionasal dysplasia RGO:26193 RGO:26194 Guadalajara camptodactyly syndrome type 1 RGO:26194 RGO:26196 MCA/MR syndrome-multiple skin creases RGO:26196 RGO:26197 Michels syndrome RGO:26197 RGO:26198 MOMES syndrome RGO:26198 ORDO:2588 SNOMEDCT:699316006 RGO:26199 Myhre syndrome RGO:26199 RGO:26201 polydactyly-absent corpus callosum-blepharophimosis RGO:26201 RGO:26203 Simosa syndrome RGO:26203 RGO:26204 tibial aplasia-polydactyly-brachyphalangy-dysmorphism-genital hypoplasia RGO:26204 RGO:26208 growth hormone insensitivity syndrome RGO:26208 DOID:11202 HP:0008200 ICD10CM:E21.0 SNOMEDCT:36348003 RGO:26210 primary hyperparathyroidism RGO:26210 pseudotumor of orbit RADLEX:RID3506 SNOMEDCT:72789009 RGO:26211 orbital pseudotumor RGO:26211 metabolic calcinosis SNOMEDCT:309760004 SNOMEDCT:84175001 RGO:26213 metastatic calcification RGO:26213 RGO:26214 invasive mucocele RGO:26214 RADLEX:RID5201 RGO:26217 optic nerve drusen RGO:26217 RGO:26221 normal trochlear apparatus RGO:26221 RGO:26224 Alves syndrome RGO:26224 cataract-microcephaly-arthrogryposis-kyphoscoliosis syndrome RGO:26225 CAMAK syndrome RGO:26225 RGO:26226 CAMFAK syndrome RGO:26226 ORDO:1373 RGO:26227 cataracts - aberrant oral frenula - growth retardation RGO:26227 RGO:26228 cataract and rhizomelic limb shortening RGO:26228 CCFDN syndrome congenital cataracts - facial dysmorphism - neuropathy syndrome ORDO:48431 RGO:26229 cataract-dysmorphism-neuropathy syndrome RGO:26229 RGO:26231 cataract-cerebellar atrophy-mental retardation-myopathy RGO:26231 Clouston hidrotic ectodermal dysplasia Fischer-Jacobsen-Clouston syndrome alopecia congenita with keratosis palmoplantaris hidrotic ectodermal dysplasia DOID:14693 SNOMEDCT:54209007 RGO:26232 Clouston syndrome RGO:26232 RGO:26233 Diaphyseal medullary stenosis with malignancy- RGO:26233 RGO:26234 Hardcastle RGO:26234 DOID:13641 RGO:26235 exfoliation syndrome RGO:26235 FOAR syndrome DOID:0090144 RGO:26236 facio-oculo-acoustico-renal syndrome RGO:26236 RGO:26238 Finlay-Marks syndrome RGO:26238 DOID:14695 ICD10CM:E74.29 ORDO:79237 SNOMEDCT:124302001 RGO:26240 galactokinase deficiency RGO:26240 RGO:26242 Gyrate atrophy with hyperornithinemia RGO:26242 ORDO:1839 SNOMEDCT:403442005 RGO:26243 hereditary mucoepithelial dysplasia RGO:26243 ORDO:163 RGO:26244 hyperferritinemia-cataract syndrome RGO:26244 HP:0003108 RGO:26245 hyperglycinuria RGO:26245 RGO:26246 hypobetalipoproteinemia and vitamin E deficiency RGO:26246 DOID:10604 HP:0004789 ICD10CM:E73 SNOMEDCT:267425008 RGO:26249 lactose intolerance RGO:26249 RGO:26250 Marginal maternal galactokinase deficiency RGO:26250 DOID:0050452 ORDO:29 SNOMEDCT:124327008 RGO:26251 Mevalonic aciduria RGO:26251 WARBM Warburg-Sjo-Fledelius syndrome DOID:0060237 ORDO:2510 RGO:26252 MICRO syndrome RGO:26252 RGO:26253 microcephaly - microphthalmia - cataract - intracranial calcification RGO:26253 RGO:26254 microcephaly - rhizomelia - cataracts - micropenis RGO:26254 RGO:26255 mitochondrial myopathy-cardiomyopathy-cataract-lactic acidosis RGO:26255 DOID:0050472 RGO:26256 Monilethrix syndrome RGO:26256 SNOMEDCT:72913007 RGO:26257 Moore-Federman syndrome RGO:26257 ORDO:35737 RGO:26258 morning glory syndrome RGO:26258 RGO:26259 oculodentoosseous syndrome RGO:26259 SNOMEDCT:699300009 RGO:26260 oculo-facio-cardio-dental syndrome RGO:26260 RGO:26261 progeroid syndrome - dysmorphism - facial erythroderma - cataracts - basal ganglia calcification - ASD RGO:26261 RGO:26262 radiculomegaly of canine teeth - cataracts RGO:26262 HP:0100504 ICD10CM:E53.0 SNOMEDCT:20307000 RGO:26263 Riboflavin deficiency RGO:26263 DOID:14692 ICD10CM:E78.72 ORDO:818 SNOMEDCT:43929004 RGO:26265 Smith-Lemli-Opitz syndrome RGO:26265 DOID:0060768 ICD10CM:Q93.88 ORDO:819 SNOMEDCT:401315004 RGO:26266 Smith-Magenis syndrome RGO:26266 RGO:26267 sorbitol dehydrogenase deficiency RGO:26267 spondylo-ocular dysplasia ORDO:85194 SNOMEDCT:715653007 RGO:26269 spondylo-ocular syndrome RGO:26269 ORDO:1410 SNOMEDCT:254230001 RGO:26270 uncombable hair syndrome RGO:26270 GALE deficiency GALE-D epimerase deficiency galactosemia galactosemia type 3 uridine diphosphate galactose-4-epimerase deficiency ORDO:79238 RGO:26271 UPD galactose-4-epimerase deficiency RGO:26271 ORDO:3437 RADLEX:RID3678 SNOMEDCT:193497004 RGO:26272 Vogt-Koyanagi-Harada syndrome RGO:26272 DOID:13098 HP:0025342 ICD10CM:H34.1 SNOMEDCT:38742007 RGO:26274 central retinal artery occlusion RGO:26274 DOID:3323 ICD10CM:E75.01 ORDO:796 SNOMEDCT:23849003 RGO:26276 Sandhoff disease RGO:26276 DOID:3320 ICD10CM:E75.02 ORDO:845 RADLEX:RID34416 SNOMEDCT:111385000 RGO:26277 Tay-Sachs disease RGO:26277 RGO:26279 macular hemorrhage RGO:26279 RGO:26280 macular hole with surrounding detachment RGO:26280 microlissencephaly type A DOID:0060902 ORDO:89844 RGO:26281 Norman-Roberts syndrome RGO:26281 RGO:26282 quinine toxicity RGO:26282 RGO:26284 traumatic retinal edema RGO:26284 RGO:26285 acrorenalocular syndrome RGO:26285 DOID:0060229 ORDO:2995 SNOMEDCT:702410002 RGO:26288 Baraitser-Winter syndrome RGO:26288 Biemond syndrome 2 ORDO:141333 RGO:26289 Biemond syndrome type 2 RGO:26289 Zunich neuroectodermal syndrome Zunich-Kaye syndrome coloboma-heart defect-ichthyosis-mental retardation-ear defect syndrome RGO:26293 CHIME syndrome RGO:26293 RGO:26294 chondrodysplasia punctata and ocular colobomata RGO:26294 RGO:26295 coloboma-radial aplasia syndrome RGO:26295 SNOMEDCT:253176002 RGO:26299 Gillespie syndrome RGO:26299 Goldberg-Shprintzen megacolon syndrome Shprintzen-Goldberg syndrome DOID:0060481 RGO:26300 Goldberg-Shprintzen syndrome RGO:26300 RGO:26302 Hirschsprung-coloboma syndrome RGO:26302 HP:0000482 RGO:26306 microcornea syndrome RGO:26306 nasopalpebral lipoma - coloboma - telecanthus palpebral coloboma-lipoma syndrome ORDO:2399 RGO:26310 nasopalpebral lipoma-coloboma syndrome RGO:26310 oculootodental syndrome RGO:26311 oculo-oto-dental syndrome RGO:26311 RGO:26312 optic nerve coloboma-renal disease RGO:26312 OFD syndrome OFDS DOID:4501 RGO:26313 orofaciodigital syndrome RGO:26313 RGO:26314 parietal bone agenesis-plus RGO:26314 RGO:26316 renal-coloboma-arthrogryposis syndrome RGO:26316 RGO:26318 Sorsby syndrome RGO:26318 SNOMEDCT:716233007 RGO:26320 Steinfeld syndrome RGO:26320 terminal osseous dysplasia with pigmentary defects RGO:26322 terminal osseous dysplasia-pigmentary defect RGO:26322 RGO:26323 white sponge nevus-ocular coloboma RGO:26323 DOID:856 ICD10CM:D81.810 ORDO:79241 SNOMEDCT:8808004 RGO:26325 biotinidase deficiency RGO:26325 DOID:9063 SNOMEDCT:200946001 RGO:26327 scalded skin syndrome RGO:26327 François syndrome dermochondrocorneal dystrophy ORDO:79149 RGO:26331 dermochondrocorneal dystrophy of François RGO:26331 ORDO:578 RGO:26336 mucolipidosis type 4 RGO:26336 ORDO:2741 SNOMEDCT:715484003 RGO:26340 ophthalmomandibulomelic dysplasia RGO:26340 DOID:0110334 ORDO:216796 RGO:26341 osteogenesis imperfecta type 1 RGO:26341 DOID:1388 ICD10CM:E78.6 ORDO:31150 SNOMEDCT:15346004 RGO:26347 Tangier disease RGO:26347 RGO:26348 chromosome 7p- syndrome RGO:26348 RGO:26349 cryptophthalmia-hypothalamic disorder RGO:26349 RGO:26350 familial nonsyndromal cryptophthalmos RGO:26350 RGO:26351 fused eyelids - subglottic stenosis - ovarian cysts - digital abnormalities RGO:26351 SNOMEDCT:57219006 RGO:26352 craniosynostosis syndrome RGO:26352 Walt Disney dwarfism geroderma osteodysplastica geroderma osteodysplasticum RGO:26354 gerodermia osteodysplastica RGO:26354 DOID:14566 HP:0002664 RADLEX:RID3957 SNOMEDCT:108369006 SNOMEDCT:55342001 RGO:26356 neoplasm RGO:26356 HP:0007476 SNOMEDCT:7731005 RGO:26360 anhidrotic ectodermal dysplasia RGO:26360 koraxitrachitic syndrome HP:0007479 ICD10CM:Q80.2 SNOMEDCT:205550003 RGO:26361 collodion baby RGO:26361 SNOMEDCT:8634009 RGO:26363 distichiasis-lymphedema syndrome RGO:26363 DOID:1459 HP:0000821 SNOMEDCT:40930008 RGO:26364 hypothyroidism RGO:26364 RGO:26372 eyelid imbrication syndrome RGO:26372 RGO:26373 floppy eyelid-sleep apnea syndrome RGO:26373 DOID:0050465 ORDO:587 RGO:26375 Muir-Torre syndrome RGO:26375 OAVS-like syndrome ORDO:1791 RGO:26376 oculo-auriculo-fronto-nasal syndrome RGO:26376 ORDO:50944 RGO:26377 Schopf-Schulz-Passarge syndrome RGO:26377 RGO:26378 Awan syndrome RGO:26378 RGO:26380 ectrodactyly-glaucoma RGO:26380 RGO:26382 familial tetralogy of Fallot and glaucoma RGO:26382 Franck-ter Haar syndrome ORDO:137834 RGO:26383 Frank-ter Haar syndrome RGO:26383 iridio-corneal-endothelial syndrome RGO:26385 ICE 2 syndrome RGO:26385 RGO:26386 mesomelic dysplasia-congenital glaucoma RGO:26386 RGO:26387 oculodentoosseous dysplasia syndrome RGO:26387 RGO:26388 PHACE association syndrome RGO:26388 RGO:26389 skeletal dysplasia and congenital glaucoma RGO:26389 acro-fronto-facio-nasal dysostosis syndrome acro-fronto-facionasal dysostosis ORDO:1784 RGO:26391 acro-fronto-facio-nasal dysostosis RGO:26391 RGO:26393 atrial septal defect-hypertelorism/cleft syndrome RGO:26393 Cenani syndactyly Cenani-Lenz syndactyly syndactyly type 7 DOID:0090015 ORDO:3258 RGO:26397 Cenani-Lenz syndactyly syndrome RGO:26397 SNOMEDCT:6936002 RGO:26399 cleft lip sequence RGO:26399 ORDO:1529 RGO:26400 craniofacial-deafness-hand syndrome RGO:26400 RGO:26402 midline dermoid RGO:26402 ORDO:2308 SNOMEDCT:715438008 RGO:26412 Jacobsen syndrome RGO:26412 DOID:3614 SNOMEDCT:93559003 RGO:26413 Kallman syndrome RGO:26413 RGO:26415 Lambotte syndrome RGO:26415 SNOMEDCT:204036008 RGO:26417 lissencephaly syndrome RGO:26417 RGO:26420 orofaciodigital syndrome type 6 RGO:26420 RGO:26427 valproate embryopathy RGO:26427 ORDO:2804 RGO:26428 W syndrome RGO:26428 ORDO:1450 RGO:26429 chromosome 8 ring RGO:26429 RGO:26430 chromosome 20p dup syndrome RGO:26430 HP:0011330 SNOMEDCT:109409003 RGO:26431 metopic craniosynostosis RGO:26431 RGO:26433 fronto-ocular syndrome RGO:26433 RGO:26437 chromosome 6p deletion RGO:26437 XP-CS ORDO:220295 RGO:26440 xeroderma pigmentosum - Cockayne syndrome complex RGO:26440 ORDO:86815 RGO:26442 agenesis-hypoplasia of salivary and lacrimal glands RGO:26442 DOID:14702 RGO:26443 branchio-otorenal dysplasia RGO:26443 RGO:26444 congenital alacrima RGO:26444 SNOMEDCT:193994000 RGO:26445 congenital nasolacrimal duct obstruction RGO:26445 RGO:26446 duplication of lacrimal punctum RGO:26446 RGO:26448 ectopic lacrimal gland tissue RGO:26448 RGO:26449 familial deficient lacrimation RGO:26449 RGO:26450 lacrimal canaliculus atresia RGO:26450 ORDO:141083 RGO:26451 lacrimal duct cyst RGO:26451 familial dysautonomia DOID:11589 RADLEX:RID5269 SNOMEDCT:29159009 RGO:26453 Riley-Day syndrome RGO:26453 RGO:26456 ectopia lentis-dysmorphism syndrome RGO:26456 DOID:13641 SNOMEDCT:44219007 RGO:26458 pseudoexfoliation syndrome RGO:26458 RGO:26459 Tuomaala syndrome RGO:26459 RGO:26460 colobomatous macrophthalmia-microcornea syndrome RGO:26460 RGO:26461 intraocular mass RGO:26461 RGO:26462 mesodermal dysplasia RGO:26462 RGO:26465 familial microspherophakia RGO:26465 DOID:9274 HP:0002161 ICD10CM:E72.3 ORDO:2203 SNOMEDCT:58558003 RGO:26466 hyperlysinemia RGO:26466 RGO:26468 camptodactyly-eye syndrome RGO:26468 SNOMEDCT:312951006 RGO:26470 multiple evanescent white dot syndrome RGO:26470 ORDO:2917 RGO:26472 polydactyly-myopia syndrome RGO:26472 craniosynostosis-radial aplasia syndrome DOID:0050654 ORDO:1225 SNOMEDCT:77608001 RGO:26474 Baller-Gerold syndrome RGO:26474 ORDO:1239 SNOMEDCT:718221007 RGO:26475 Behr syndrome RGO:26475 BFLS intellectual deficiency - epilepsy - endocrine disorders DOID:0050681 ORDO:127 SNOMEDCT:21634003 RGO:26477 Börjeson-Forssman-Lehmann syndrome RGO:26477 ORDO:2329 RGO:26479 Karsch-Neugebauer syndrome RGO:26479 RGO:26483 parietal foramina-multiple exostosis RGO:26483 SNOMEDCT:37991008 RGO:26484 Parinaud syndrome RGO:26484 ORDO:3020 RGO:26485 Ramsay-Hunt syndrome RGO:26485 RGO:26487 X-linked congenital nystagmus RGO:26487 RGO:26488 skin creases RGO:26488 RGO:26491 familial microtia RGO:26491 HP:0002079 RGO:26492 hypoplastic corpus callosum RGO:26492 HP:0000384 SNOMEDCT:204245004 RGO:26493 preauricular tag RGO:26493 RGO:26494 characteristic facies RGO:26494 HP:0004467 RGO:26495 preauricular pits RGO:26495 HP:0004209 RGO:26496 fifth finger clinodactyly RGO:26496 DOID:6419 HP:0001636 ICD10CM:Q21.3 ORDO:3303 RADLEX:RID34611 SNOMEDCT:86299006 RGO:26497 tetralogy of Fallot RGO:26497 HP:0000284 RGO:26498 ocular abnormalities RGO:26498 RGO:26499 oligophrenia RGO:26499 HP:0000528 SNOMEDCT:7183006 RGO:26500 anophthalmia RGO:26500 HP:0000272 RGO:26501 malar hypoplasia RGO:26501 HP:0000233 SNOMEDCT:301348000 RGO:26502 thin lips RGO:26502 RGO:26503 long tapering fingers RGO:26503 HP:0001263 SNOMEDCT:398991009 RGO:26504 psychomotor retardation RGO:26504 RGO:26506 external ear anomaly RGO:26506 RGO:26508 long thin face RGO:26508 HP:0008551 RGO:26509 small ears RGO:26509 RGO:26510 brachycamptodactyly RGO:26510 RGO:26511 persistent wormian bones RGO:26511 HP:0000347 ICD10CM:M26.04 RGO:26512 mandibular hypoplasia RGO:26512 HP:0006487 RGO:26514 camptomelia RGO:26514 RGO:26515 optic nerve trauma RGO:26515 SNOMEDCT:277002002 RGO:26516 rod defect RGO:26516 SNOMEDCT:277003007 RGO:26517 cone defect RGO:26517 HP:0000612 RGO:26518 iris coloboma RGO:26518 RGO:26519 broad and flat nasal bridge RGO:26519 HP:0000537 SNOMEDCT:400956000 RGO:26520 epicanthus inversus RGO:26520 RGO:26523 fovea hypoplasia RGO:26523 RGO:26524 bony syngnathia RGO:26524 HP:0001116 RGO:26529 macular coloboma RGO:26529 DOID:674 HP:0000175 ICD10CM:Q35 ORDO:2014 SNOMEDCT:87979003 RGO:26530 cleft palate RGO:26530 RGO:26532 siblings RGO:26532 HP:0000567 SNOMEDCT:39302008 RGO:26533 chorioretinal coloboma RGO:26533 HP:0001274 ICD10CM:Q04.0 SNOMEDCT:5102002 RGO:26534 agenesis of corpus callosum RGO:26534 HP:0002119 SNOMEDCT:413808003 RGO:26535 ventriculomegaly RGO:26535 HP:0000280 RGO:26537 coarse face RGO:26537 RGO:26538 temporal cutis aplasia RGO:26538 RGO:26539 double upper eyelashes RGO:26539 HP:0007646 RGO:26540 absent lower eyelashes RGO:26540 DOID:2475 ICD10CM:H10.4 SNOMEDCT:73762008 RGO:26541 chronic conjunctivitis RGO:26541 HP:0012471 RGO:26542 thick lips RGO:26542 HP:0008527 SNOMEDCT:95828007 RGO:26545 congenital sensorineural deafness RGO:26545 RGO:26546 low plasma levels of apolipoprotein A-I and high-density lipoprotein cholesterol RGO:26546 RGO:26547 accumulation of cholesteryl esters in tissues RGO:26547 DOID:574 DOID:870 HP:0009830 SNOMEDCT:302226006 RGO:26548 peripheral neuropathy RGO:26548 DOID:2566 HP:0001131 SNOMEDCT:5587004 RGO:26549 corneal dystrophy RGO:26549 HP:0000212 RGO:26550 gum hypertrophy RGO:26550 RGO:26551 unerupted teeth RGO:26551 RGO:26552 resorption of unerupted teeth RGO:26552 RGO:26558 vertebral ankylosis RGO:26558 ORDO:3266 RGO:26559 humero-radial-ulnar ankylosis RGO:26559 RGO:26560 intercarpal ankylosis RGO:26560 RGO:26561 interphalangeal ankylosis RGO:26561 RGO:26562 tibiofibular ankylosis RGO:26562 RGO:26564 bitemporal scar-like skin defects RGO:26564 RGO:26566 fleshy nose RGO:26566 HP:0100540 RGO:26567 eyelid edema RGO:26567 RGO:26569 sagging eyelid RGO:26569 RGO:26570 swelling of the upper lip RGO:26570 RGO:26571 double upper lip RGO:26571 HP:0000154 ICD10CM:Q18.4 SNOMEDCT:40159009 RGO:26572 macrostomia RGO:26572 DOID:3390 HP:0000982 SNOMEDCT:706885006 RGO:26574 palmoplantar keratoderma RGO:26574 RGO:26575 teeth/hair nail dystrophy RGO:26575 RGO:26576 lean physique RGO:26576 RGO:26577 lens ectopia RGO:26577 HP:0001387 SNOMEDCT:84445001 RGO:26578 joint stiffness RGO:26578 HP:0004322 SNOMEDCT:237836003 RGO:26579 short stature RGO:26579 HP:0006487 RGO:26581 bowed long bones RGO:26581 RGO:26582 finger flexion deformity RGO:26582 RGO:26584 Noonan-like phenotype RGO:26584 SNOMEDCT:77746001 RGO:26586 leontiasis RGO:26586 HP:0001480 RGO:26587 freckling RGO:26587 HP:0002164 RGO:26588 nail dysplasia RGO:26588 HP:0006357 RGO:26589 early loss of permanent teeth RGO:26589 RGO:26590 neurodermitic signs RGO:26590 RGO:26591 obstructed lacrimal ducts RGO:26591 HP:0002557 RGO:26592 nipple hypoplasia RGO:26592 HP:0000522 SNOMEDCT:253215004 RGO:26594 alacrima RGO:26594 HP:0001492 ORDO:98978 SNOMEDCT:204152008 RGO:26595 Axenfeld anomaly RGO:26595 DOID:10003 HP:0000407 SNOMEDCT:60700002 RGO:26596 sensorineural hearing loss RGO:26596 RGO:26598 progressive myopia RGO:26598 RGO:26601 Foster Kennedy syndrome RGO:26601 RGO:26607 optic tract syndrome RGO:26607 ORDO:2836 RGO:26608 PEHO syndrome RGO:26608 ORDO:320406 RGO:26610 spastic paraplegia-optic atrophy-neuropathy syndrome RGO:26610 DOID:2385 HP:0100503 SNOMEDCT:399357009 RGO:26611 vitamin B1 deficiency RGO:26611 buphthalmos HP:0001087 ICD10CM:Q15.0 ORDO:98976 SNOMEDCT:204113001 RGO:26613 congenital glaucoma RGO:26613 microphthalmos DOID:10629 HP:0000568 SNOMEDCT:61142002 RGO:26614 microphthalmia RGO:26614 Adamentiades-Behçet syndrome Behçet syndrome Gilbert-Behçet syndrome l'aphthose de Touraine RGO:26615 Behçet disease RGO:26615 DOID:0050848 SNOMEDCT:78275009 RGO:26616 obstructive sleep apnea syndrome RGO:26616 ICD10CM:E66.2 SNOMEDCT:190966007 RGO:26617 Pickwickian syndrome RGO:26617 RGO:26619 pseudotumor cerebri syndrome RGO:26619 SNOMEDCT:450886002 RGO:26620 reversible posterior leukoencephalopathy syndrome RGO:26620 RGO:26626 congenital dyserythropoetic anemia-plus RGO:26626 RGO:26627 congenital ptosis-congenital heart disease RGO:26627 RGO:26633 lymphedema-ptosis syndrome RGO:26633 reverse Marcus-Gunn syndrome ORDO:101104 RGO:26634 Marin-Amat syndrome RGO:26634 ORDO:298 RGO:26635 mitochondrial-neurogastrointestinal-encephalomyopathy RGO:26635 RGO:26637 myasthenia syndrome RGO:26637 RGO:26639 Raeder syndrome RGO:26639 DOID:0050661 RGO:26642 Best macular dystrophy RGO:26642 DOID:0060349 RGO:26644 chorioretinal dysplasia-microcephaly-mental retardation syndrome RGO:26644 RGO:26647 familial hematuria-retinal arteriolar tortuosity-contracture syndrome RGO:26647 RGO:26651 Gurrieri syndrome RGO:26651 RGO:26653 hereditary endotheliopathy RGO:26653 RGO:26654 hereditary retinal vasculopathy with cerebral white matter lesions RGO:26654 RGO:26656 ichthyosiform erythroderma and retinitis pigmentosa RGO:26656 DOID:14791 ORDO:65 SNOMEDCT:193413001 RGO:26659 Leber congenital amaurosis RGO:26659 SNOMEDCT:312941005 RGO:26660 melanoma-associated retinopathy RGO:26660 DOID:0060844 ORDO:649 RGO:26663 Norrie disease RGO:26663 RGO:26667 retinitis pigmentosa and basal ganglia calcification RGO:26667 RGO:26669 Révész syndrome RGO:26669 RGO:26670 rhizomelic bone dysplasia with retinitis pigmentosa RGO:26670 RGO:26675 hydroxy-dicarboxylic aciduria RGO:26675 DOID:14503 ICD10CM:E75.4 ORDO:216 SNOMEDCT:42012007 RGO:26676 neuronal ceroid lipofuscinosis RGO:26676 SNOMEDCT:276426004 RGO:26677 ornithine aminotransferase deficiency RGO:26677 DOID:10582 ORDO:773 RGO:26679 Refsum disease RGO:26679 ORDO:959 RGO:26680 acro-renal-ocular syndrome RGO:26680 RGO:26684 diffuse leukodystrophy RGO:26684 HP:0007957 RGO:26685 corneal clouding RGO:26685 RGO:26686 iridolenticulocorneal adhesions RGO:26686 HP:0001510 RGO:26687 growth deficiency RGO:26687 RGO:26688 small distal phalanges RGO:26688 HP:0001285 SNOMEDCT:298282001 RGO:26689 spastic quadriparesis RGO:26689 RGO:26690 progressive joint contractures RGO:26690 HP:0001258 SNOMEDCT:192967009 RGO:26691 spastic paraplegia RGO:26691 RGO:26696 partial agenesis of the abdominal musculature with diastasis recti RGO:26696 HP:0001488 RGO:26699 bilateral ptosis RGO:26699 HP:0000544 SNOMEDCT:19373007 RGO:26700 external ophthalmoplegia RGO:26700 HP:0000494 RGO:26701 down-slanting palpebral fissures RGO:26701 HP:0000171 ICD10CM:Q38.3 SNOMEDCT:32614006 RGO:26702 hypoglossia RGO:26702 RGO:26703 Pierre Robin anomaly RGO:26703 RGO:26705 congenital ocular fibrosis RGO:26705 HP:0002579 RGO:26706 gastrointestinal dysmotility RGO:26706 DOID:644 HP:0002352 SNOMEDCT:22811006 RGO:26707 leukoencephalopathy RGO:26707 DOID:0090070 DOID:1921 ICD10CM:E23.0 SNOMEDCT:33927004 RGO:26708 hypogonadotropic hypogonadism RGO:26708 DOID:8466 HP:0000546 SNOMEDCT:95695004 RGO:26709 retinal degeneration RGO:26709 RGO:26710 neurogenic deafness RGO:26710 DOID:9970 HP:0001513 RADLEX:RID11305 SNOMEDCT:414916001 RGO:26711 obesity RGO:26711 DOID:6713 HP:0001297 RADLEX:RID5178 SNOMEDCT:230690007 RGO:26712 stroke RGO:26712 HP:0000303 SNOMEDCT:72855002 RGO:26714 prognathism RGO:26714 RGO:26715 narrow retinal arteries RGO:26715 RGO:26716 central nervous system abnormality RGO:26716 RGO:26718 cerebral dysplasia RGO:26718 DOID:1074 RGO:26720 kidney failure RGO:26720 HP:0011001 RGO:26722 increased bone density RGO:26722 SNOMEDCT:276720006 RGO:26724 dysmorphism RGO:26724 RGO:26725 foot anomaly RGO:26725 RGO:26728 oculo-ectodermal syndrome RGO:26728 ORDO:2749 RGO:26731 oromandibular-limb hypogenesis syndrome RGO:26731 Aarskog-Scott syndrome FDG syndrome faciodigitogenital syndrome DOID:6683 ICD10CM:Q87.1 SNOMEDCT:14921002 RGO:26733 Aarskog syndrome RGO:26733 ablepharon-macrostomia syndrome DOID:0060550 ORDO:920 RGO:26734 ablepharon macrostomia syndrome RGO:26734 cardiofaciocutaneous syndrome SNOMEDCT:403770008 RGO:26737 cardio-facio-cutaneous syndrome RGO:26737 RGO:26739 chromosome 3q1 disorder RGO:26739 RGO:26740 chromosome 9q deletion RGO:26740 RGO:26741 chromosome 10p deletion RGO:26741 RGO:26742 chromosome 10q1 disorder RGO:26742 RGO:26743 chromosome 12p1 disorder RGO:26743 Edwards syndrome DOID:1085 ORDO:3380 RADLEX:RID46045 RGO:26744 trisomy 18 RGO:26744 Ehlers-Danlos syndrome progeroid form DOID:0050802 ORDO:75496 RGO:26746 Ehlers-Danlos syndrome progeroid type RGO:26746 ORDO:1913 SNOMEDCT:66351003 RGO:26747 fetal trimethadione syndrome RGO:26747 DOID:0060831 ORDO:381 SNOMEDCT:37548006 RGO:26750 Griscelli syndrome RGO:26750 familial acro-osteolysis idiopathic acro-osteolysis DOID:2736 SNOMEDCT:63122002 RGO:26751 Hajdu-Cheney syndrome RGO:26751 SNOMEDCT:403799003 RGO:26754 hypertrichosis universalis congenita RGO:26754 ichthyosis-cheek-eyebrow syndrome RGO:26755 ICE 1 syndrome RGO:26755 keratitis-ichthyosis-deafness syndrome ORDO:477 SNOMEDCT:239059004 RGO:26761 KID syndrome RGO:26761 DOID:0110949 RGO:26762 Klein-Waardenburg syndrome RGO:26762 DOID:0050472 ICD10CM:Q84.1 ORDO:573 RGO:26766 monilethrix RGO:26766 MPS 6 Maroteaux-Lamy syndrome ORDO:583 RGO:26769 mucopolysaccharidosis type 6 RGO:26769 RGO:26772 partial eyebrow duplication-multiple malformation syndrome RGO:26772 RGO:26774 restrictive dermatopathy RGO:26774 RGO:26781 unusual facies-arthrogryposis-advanced skeletal maturation syndrome RGO:26781 Williams-Beuren syndrome idiopathic hypercalcemia ORDO:904 SNOMEDCT:63247009 RGO:26784 Williams syndrome RGO:26784 familial fibrous dysplasia of the jaw DOID:1856 ICD10CM:M27.8 ORDO:184 RADLEX:RID3739 SNOMEDCT:76098004 RGO:26785 cherubism RGO:26785 RGO:26786 Noonan-like syndrome RGO:26786 ORDO:3019 RGO:26787 Ramon syndrome RGO:26787 ORDO:1241 RGO:26788 Bencze syndrome RGO:26788 RGO:26792 HATS syndrome RGO:26792 DOID:2907 HP:0011332 ORDO:141136 SNOMEDCT:254025006 RGO:26793 hemifacial microsomia RGO:26793 RGO:26794 familial hemifacial microsomia with radial limb defect RGO:26794 SNOMEDCT:708674003 RGO:26796 hemimaxillofacial dysplasia RGO:26796 ORDO:71276 SNOMEDCT:699802009 RGO:26801 silent sinus syndrome RGO:26801 HP:0100731 RGO:26803 lateral facial cleft RGO:26803 median cleft upper lip RGO:26804 median cleft of the upper lip RGO:26804 ORDO:2006 RGO:26806 median mandibular cleft RGO:26806 RGO:26807 oblique facial cleft RGO:26807 RGO:26813 mandibulofacial dysostosis and tibial hemimelia RGO:26813 RGO:26815 maxillofacial dysostosis RGO:26815 RGO:26819 oral-acral anomaly Verloes-Koulischer type RGO:26819 RGO:26820 otopalatodigital dysplasia type 2 RGO:26820 RGO:26822 Pierpont syndrome RGO:26822 spondyloepimetaphyseal dysplasia short limb - abnormal calcification type RGO:26824 spondyloepimetaphyseal dysplasia short limb-hand abnormal calcification type RGO:26824 RGO:26825 tattoo dysplasia RGO:26825 3M syndrome MMM syndrome Miller-McKusick-Malvaux syndrome dolichospondylic dysplasia gloomy face syndrome le Merrer syndrome three M syndrome DOID:0060241 ORDO:2616 SNOMEDCT:702342007 RGO:26826 3-M syndrome RGO:26826 ORDO:958 RGO:26828 acro-renal-mandibular syndrome RGO:26828 RGO:26829 acro-renal-uterine-mandibular syndrome RGO:26829 RGO:26831 agnathia malformation complex RGO:26831 ORDO:1790 RGO:26833 hypomandibular faciocranial dysostosis RGO:26833 RGO:26836 oral-acral syndrome Verloes-Koulischer type RGO:26836 DOID:6686 RGO:26838 Achard syndrome RGO:26838 RGO:26839 acrorenal-mandibular syndrome RGO:26839 RGO:26840 bifid epiglottis syndrome RGO:26840 ORDO:1406 RGO:26841 Charlie M syndrome RGO:26841 Cole-Carpenter dysplasia DOID:0060438 ORDO:2050 RGO:26846 Cole-Carpenter syndrome RGO:26846 ORDO:1512 RGO:26848 Crane-Heise syndrome RGO:26848 genito-palato-cardiac syndrome RGO:26851 Gardner-Silengo-Wachtel syndrome RGO:26851 ORDO:141163 SNOMEDCT:89444000 RGO:26852 glossopalatine ankylosis syndrome RGO:26852 ORDO:2097 RGO:26853 Grant syndrome RGO:26853 oculocerebrofacial syndrome Kaufman type ORDO:2707 RGO:26854 Kaufman oculocerebrofacial syndrome RGO:26854 Lenz-Majewski hyperostotic dwarfism Lenz-Majewski hyperostotic dysplasia Lenz-Majewski syndrome hyperostotic dwarfism SNOMEDCT:1393001 RGO:26855 Lenz-Majewski dysplasia RGO:26855 ORDO:2872 RGO:26860 Pfeiffer-type cardiocranial syndrome RGO:26860 RGO:26861 postaxial acrofacial dysostosis syndrome Miller type RGO:26861 ORDO:3104 RGO:26862 Robin sequence and oligodactyly RGO:26862 RGO:26863 Rutledge syndrome RGO:26863 RGO:26869 Ehlers-Danlos syndrome type 4 RGO:26869 Worth type osteosclerosis RGO:26870 endosteal hyperostosis Worth type RGO:26870 RGO:26871 familial prognathism RGO:26871 RGO:26874 hyperostosis generalisata with bone striation RGO:26874 RGO:26875 LAPS syndrome RGO:26875 SNOMEDCT:254137006 RGO:26879 oculodento-osseous dysplasia RGO:26879 ORDO:2864 RGO:26883 short stature, mandibular prognathism, and short femoral necks RGO:26883 ORDO:1072 RGO:26885 ankyloblepharon filiforme adnatum and cleft lip/palate RGO:26885 cleft palate-cardiac defect-genital anomaly-ectrodactyly syndrome RGO:26890 CCGE syndrome RGO:26890 ORDO:2016 RGO:26892 cleft palate-lateral synechiae syndrome RGO:26892 RGO:26893 familial cleft uvula RGO:26893 RGO:26896 Fontaine syndrome RGO:26896 RGO:26898 Hardikar syndrome RGO:26898 RGO:26900 Hermann syndrome RGO:26900 RGO:26902 isolated cleft lip RGO:26902 RGO:26904 laryngotracheoesophageal cleft and cleft palate RGO:26904 ORDO:86917 RGO:26906 lymphedema in association with cleft palate RGO:26906 Gypsy type facial clefting syndrome Malpuech facial clefting syndrome RGO:26907 Malpuech syndrome RGO:26907 RGO:26908 MCA syndrome RGO:26908 RGO:26911 microcephaly-facial clefting-polydactyly syndrome RGO:26911 RGO:26912 odontotrichomelic hypohidrotic dysplasia RGO:26912 RGO:26913 familial oligodactyly and Robin sequence RGO:26913 ORDO:1993 RGO:26919 Pai syndrome RGO:26919 RGO:26922 Phillips-Griffiths syndrome RGO:26922 Robin sequence-aniridia-growth retardation syndrome RGO:26923 RAG syndrome RGO:26923 DOID:0050774 ORDO:3021 SNOMEDCT:702413000 RGO:26924 RAPADILINO syndrome RGO:26924 ORDO:2353 RGO:26928 Schilbach-Rott syndrome RGO:26928 short rib syndrome Beemer-Langer type RGO:26931 short rib syndrome type 4 RGO:26931 DOID:0060239 ORDO:888 SNOMEDCT:79261008 RGO:26933 van der Woude syndrome RGO:26933 ORDO:1253 SNOMEDCT:28599006 RGO:26934 Ascher syndrome RGO:26934 DOID:0060563 ORDO:46627 SNOMEDCT:703534001 RGO:26936 CHAR syndrome RGO:26936 RGO:26942 lethal congenital dwarfism with accelerated maturation RGO:26942 RGO:26945 chromosome 5p- RGO:26945 RGO:26946 chromosome 18q2 monosomy RGO:26946 Chudley-Lowry-Hoar syndrome ORDO:93971 RGO:26947 Chudley-Lowry syndrome RGO:26947 RGO:26948 macrostomia - mental retardation - hyperpnea syndrome RGO:26948 RGO:26951 extreme microglossia RGO:26951 RGO:26954 agnathia-synotia-microstomia syndrome RGO:26954 windmill-vane camptodactyly DOID:0050646 HP:0005684 SNOMEDCT:24269006 RGO:26955 distal arthrogryposis RGO:26955 Burton dysplasia Kniest-like syndrome with pursed lips and ectopia lentis DOID:0090005 RGO:26956 Burton syndrome RGO:26956 DOID:0060341 ICD10CM:Q18.2 SNOMEDCT:48180002 RGO:26960 otocephaly RGO:26960 RGO:26964 agenesis/hypoplasia of the salivary glands RGO:26964 DOID:7365 ORDO:482 RADLEX:RID3480 SNOMEDCT:399894006 RGO:26965 Kimura disease RGO:26965 EMG syndrome Wiedemann-Beckwith syndrome exomphalos-macroglossia-gigantism syndrome DOID:5572 ICD10CM:Q87.3 ORDO:116 SNOMEDCT:81780002 RGO:26967 Beckwith-Wiedemann syndrome RGO:26967 HP:0010297 SNOMEDCT:204630003 RGO:26970 cleft tongue RGO:26970 DKC Zinsser-Engman-Cole syndrome dyskeratosis congenita syndrome DOID:2729 ORDO:1775 SNOMEDCT:74911008 RGO:26972 dyskeratosis congenita RGO:26972 DOID:11514 HP:0000221 ICD10CM:K14.5 SNOMEDCT:52368004 RGO:26974 fissured tongue RGO:26974 RGO:26977 isolated tongue hemiatrophy RGO:26977 ORDO:2319 RGO:26979 Juberg-Hayward syndrome RGO:26979 congenital hyperuricosuria DOID:1919 ICD10CM:E79.1 ORDO:510 SNOMEDCT:10406007 RGO:26981 Lesch-Nyhan syndrome RGO:26981 DOID:0050778 ORDO:564 RGO:26983 Meckel syndrome RGO:26983 DOID:1761 ICD10CM:G51.2 ORDO:2483 SNOMEDCT:37770007 RGO:26984 Melkersson-Rosenthal syndrome RGO:26984 RGO:26987 neck-tongue syndrome RGO:26987 Stueve-Wiedemann dysplasia ORDO:3206 SNOMEDCT:254097005 RGO:26993 Stüve-Wiedemann dysplasia RGO:26993 RGO:26997 choanal-adenoid syndrome RGO:26997 RGO:26999 choanal atresia and lymphedema RGO:26999 RGO:27000 choanal-ileal atresia association RGO:27000 DOID:0060055 SNOMEDCT:718222000 RGO:27002 facio-genito-popliteal syndrome RGO:27002 RGO:27003 familial choanal atresia RGO:27003 ORDO:1923 RGO:27004 methimazole embryopathy RGO:27004 RGO:27005 radial ray hypoplasia syndrome RGO:27005 ORDO:798 SNOMEDCT:18899000 RGO:27006 Schinzel-Giedion syndrome RGO:27006 RGO:27010 familial bifid nose RGO:27010 ORDO:2378 RGO:27012 Laurin-Sandrow syndrome RGO:27012 RGO:27013 median cleft nose RGO:27013 RGO:27019 hereditary agenesis of nasal cartilage RGO:27019 SNOMEDCT:53974002 RGO:27024 Kniest syndrome RGO:27024 RGO:27025 lethal micromelic-facial bones sclerosis dysplasia RGO:27025 RGO:27030 skeletal dysplasia-Opalescent/Rootless Teeth *** RGO:27030 RGO:27031 azoospermia-nasal polyposis syndrome RGO:27031 RGO:27033 Brooks-Wiesnewski-Brown syndrome RGO:27033 ORDO:157832 RGO:27035 craniorhiny RGO:27035 RGO:27036 Hernandez syndrome RGO:27036 Laband syndrome Laband-Zimmermann syndrome ZLS ORDO:3473 SNOMEDCT:699447001 RGO:27042 Zimmermann-Laband syndrome RGO:27042 RGO:27046 familial progressive nasal alar collapse RGO:27046 HP:0003414 RGO:27048 atlantoaxial dislocation RGO:27048 SNOMEDCT:31785008 RGO:27049 Collet-Sicard syndrome RGO:27049 RGO:27053 unfused C1 posterior arch RGO:27053 RGO:27054 autosomal dominant craniosynostosis Warman type RGO:27054 RGO:27055 Beare-Stevenson syndrome RGO:27055 RGO:27056 campomelic dysplasia craniosynostosis type RGO:27056 RGO:27057 chromosome 13q duplication RGO:27057 RGO:27058 chromosome 15q duplication RGO:27058 RGO:27059 cloverleaf skull-limb anomalies RGO:27059 Childrens Orthopedic Hospital syndrome RGO:27060 COH syndrome RGO:27060 SNOMEDCT:715434005 RGO:27061 Genoa syndrome RGO:27061 RGO:27062 hydrocephalus after shunting RGO:27062 RGO:27063 Say-Poznanski syndrome RGO:27063 RGO:27064 acrocephalosynakie RGO:27064 RGO:27067 Armendares syndrome RGO:27067 RGO:27068 auralcephalosyndactyly RGO:27068 RGO:27069 aurodigital-anal syndrome RGO:27069 RGO:27072 Calabro syndrome RGO:27072 RGO:27076 Congenital hemolytic icterus RGO:27076 ORDO:1516 RGO:27079 craniofacial dyssynostosis RGO:27079 RGO:27081 craniosynostosis-ectopia lentis RGO:27081 ORDO:1527 RGO:27084 craniosynostosis Philadelphia type RGO:27084 ORDO:1553 RGO:27085 Curry-Jones syndrome RGO:27085 RGO:27087 chromosome del(7p) syndrome RGO:27087 acrocephalopolydactylous dysplasia RGO:27088 Elejalde syndrome 1 RGO:27088 RGO:27089 familial craniosynostosis RGO:27089 RGO:27091 fluconazole embryopathy RGO:27091 RGO:27092 Fontaine-Farriaux syndrome RGO:27092 RGO:27093 Frydman trigonocephaly syndrome RGO:27093 RGO:27095 Hersh syndrome RGO:27095 RGO:27097 humeroradioulnar synostosis and lambdoid synostosis RGO:27097 MPS 2 iduronate sulfatase deficiency mucopolysaccharidosis type 2 DOID:12799 SNOMEDCT:70737009 RGO:27098 Hunter syndrome RGO:27098 RGO:27099 Hurst syndrome RGO:27099 RGO:27101 hypophosphatasemia RGO:27101 RGO:27102 Idaho syndrome RGO:27102 RGO:27103 chromosome interstitial deletion of 8q13.3-22.1 RGO:27103 ORDO:1540 SNOMEDCT:709105005 RGO:27105 Jackson-Weiss syndrome RGO:27105 RGO:27106 Jones syndrome RGO:27106 RGO:27107 Lowry syndrome RGO:27107 ORDO:2409 RGO:27108 Lowry-MacLean syndrome RGO:27108 RGO:27109 Mercedes Benz syndrome RGO:27109 DOID:0110339 ORDO:216812 RGO:27110 osteogenesis imperfecta type 3 RGO:27110 RGO:27111 parietal foramina-clavicular hypoplasia dysplasia-like syndrome RGO:27111 RGO:27112 Pfeiffer cardiocranial syndrome RGO:27112 RGO:27113 Pfeiffer-type dolichocephalosyndactyly RGO:27113 RGO:27115 Say-Barber syndrome RGO:27115 ORDO:3134 RGO:27117 SCARF syndrome RGO:27117 RGO:27120 Thanos syndrome RGO:27120 RGO:27121 Ventruto syndrome RGO:27121 RGO:27122 X-linked calvarial hyperostosis and premature cranial synostosis RGO:27122 DOID:14737 SNOMEDCT:715421009 RGO:27123 craniofrontonasal syndrome RGO:27123 RGO:27125 familial cranium bifidum occultum RGO:27125 RGO:27126 frontal bone defect RGO:27126 RGO:27128 aplasia cutis congenita of the scalp RGO:27128 craniosynostosis-anal anomaly-porokeratosis syndrome RGO:27129 CDAGS syndrome RGO:27129 RGO:27130 chromosome syndrome RGO:27130 ORDO:85184 RGO:27131 craniometadiaphyseal dysplasia Wormian bone type RGO:27131 RGO:27133 Marfanoid habitus and patent fontanelles in adulthood RGO:27133 Currarino syndrome RGO:27134 familial idiopathic osteoarthropathy RGO:27134 RGO:27135 Raine syndrome RGO:27135 RGO:27137 Wiedemann syndrome RGO:27137 RGO:27138 frontofacial syndrome RGO:27138 condylus occipitalis RGO:27139 median occipital condyle RGO:27139 RGO:27140 Antley-Bixler-like syndrome RGO:27140 RGO:27142 Holt-Oram-like syndrome RGO:27142 RGO:27143 IMAGe association RGO:27143 RGO:27149 parietal foramina-clavicular hypoplasia dysplasia RGO:27149 ORDO:965 RGO:27151 acromegaloid facial appearance syndrome RGO:27151 RGO:27152 agenesis of corpus callosum and macrocephaly RGO:27152 RGO:27154 benign macrocephaly of infancy RGO:27154 RGO:27156 cerebro-osseous-digital syndrome RGO:27156 RGO:27159 Clark-Baraitser syndrome RGO:27159 RGO:27160 Cole-Hughes macrocephaly syndrome RGO:27160 SNOMEDCT:278833002 RGO:27161 craniometadiaphyseal dysplasia RGO:27161 RGO:27163 Raine-like desmosterolosis RGO:27163 RGO:27165 chromosome 1q duplication syndrome RGO:27165 RGO:27166 chromosome 5p duplication syndrome RGO:27166 SNOMEDCT:253168004 RGO:27167 familial megalencephaly RGO:27167 RGO:27169 frontonasal syndrome RGO:27169 RGO:27171 hemicerebral arterial ectasia RGO:27171 RGO:27173 hemimegalencephaly and neonatal high-output cardiac failure RGO:27173 RGO:27177 linear sebaceous nevus syndrome and unilateral megalencephaly RGO:27177 RGO:27178 macrocephaly-cutis marmorata telangiectasia syndrome RGO:27178 RGO:27181 megencephalic leukoencephalopathy RGO:27181 megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome RGO:27182 MPPH syndrome RGO:27182 RGO:27186 multiple hemangiomatosis syndrome RGO:27186 RGO:27187 N-acetylaspartic aciduria RGO:27187 ORDO:2673 RGO:27188 neurofaciodigitorenal syndrome RGO:27188 RGO:27191 overgrowth syndrome RGO:27191 DOID:0050629 ORDO:51 RGO:27195 Aicardi-Goutiéres syndrome RGO:27195 RGO:27196 atelencephalic microcephaly RGO:27196 DOID:14725 ORDO:2514 RGO:27197 autosomal dominant microcephaly RGO:27197 pseudo-TORCH syndrome RGO:27201 Baraitser-Reardon syndrome RGO:27201 Senior syndrome ORDO:1292 RGO:27204 brachymorphism-onychodysplasia-dysphalangism syndrome RGO:27204 RGO:27205 cerebellar hypoplasia with endosteal sclerosis RGO:27205 RGO:27212 familial microcephaly RGO:27212 ORDO:3255 RGO:27216 Filippi syndrome RGO:27216 RGO:27231 microcephaly-rib gap syndrome RGO:27231 RGO:27234 Mutchinick syndrome RGO:27234 DOID:7400 ORDO:647 SNOMEDCT:234638009 RGO:27236 Nijmegen breakage syndrome RGO:27236 RGO:27237 oculopalatocerebral syndrome RGO:27237 HP:0002928 SNOMEDCT:46683007 RGO:27238 pyruvate dehydrogenase complex deficiency RGO:27238 DOID:0060179 ORDO:3242 SNOMEDCT:699669001 RGO:27239 Renpenning syndrome RGO:27239 DOID:0060356 ORDO:1493 RGO:27243 Vici syndrome RGO:27243 RGO:27246 dental-skeletal syndrome RGO:27246 RGO:27248 MOPD Kantaputra type RGO:27248 Golabi-Rosen syndrome gigantism-dysplasia syndrome DOID:0060248 ORDO:373 SNOMEDCT:439143004 RGO:27249 Simpson-Golabi-Behmel syndrome RGO:27249 RGO:27250 sterno-costo-clavicular hyperostosis RGO:27250 SNOMEDCT:447169001 RGO:27252 cranial fasciitis RGO:27252 RGO:27254 plagiocephaly-craniofacial dysmorphism-mental retardation RGO:27254 ORDO:945 RGO:27255 acalvaria RGO:27255 RGO:27257 congenital frontal bone defect with intact overlying scalp RGO:27257 RGO:27260 familial skull doughnut lesion RGO:27260 Astley-Kendall dysplasia RGO:27263 lethal osteosclerotic skeletal dysplasia Astley-Kendall type RGO:27263 RGO:27265 Schinzel phocomelia RGO:27265 RGO:27267 cyanotic congenital heat disease with polycythemia RGO:27267 RGO:27270 familial hyperostosis cranialis interna RGO:27270 RGO:27271 X-linked familial calvarial hyperostosis RGO:27271 Albright disease fibrous dysplasia polyostotic form DOID:1858 HP:0010735 ICD10CM:Q78.1 ORDO:93276 RADLEX:RID34709 SNOMEDCT:36517007 RGO:27276 polyostotic fibrous dysplasia RGO:27276 RGO:27278 hyperostosis generalisata RGO:27278 RGO:27280 panostotic fibrous dysplasia RGO:27280 RGO:27286 chromosome 9p-like syndrome RGO:27286 RGO:27287 familial trigonocephaly RGO:27287 Say-Meyer trigonocephaly syndrome RGO:27288 Say-Meyer syndrome RGO:27288 RGO:27290 sporadic trigonocephaly RGO:27290 DOID:0060231 ORDO:2771 SNOMEDCT:254113006 RGO:27294 Bruck syndrome RGO:27294 RGO:27297 craniometaphyseal dysplasia Wormian bone type RGO:27297 RGO:27300 infantile-type osteopetrosis RGO:27300 RGO:27301 oto-facio-osseous-gonadal syndrome RGO:27301 RGO:27303 angel-shaped phalangoepiphyseal dysplasia RGO:27303 ORDO:1262 RGO:27304 Böök syndrome RGO:27304 ORDO:2067 RGO:27305 GAPO syndrome RGO:27305 RGO:27306 Grebe-like chondrodysplasia RGO:27306 dermatoosteolysis Kirghizian type ORDO:1657 RGO:27309 Kirghizian dermato-osteolysis RGO:27309 ORDO:2721 SNOMEDCT:403762003 RGO:27310 odonto-onycho-dermal dysplasia RGO:27310 ORDO:2723 SNOMEDCT:239028001 RGO:27311 odontotrichomelic syndrome RGO:27311 oro-palatal syndrome Bettex-Graf type RGO:27312 oro-palatal dysplasia Bettex-Graf type RGO:27312 DOID:0050475 ORDO:3449 SNOMEDCT:2884008 RGO:27316 Weill-Marchesani syndrome RGO:27316 RGO:27317 Witkop tooth-nail syndrome RGO:27317 oculodental syndrome Rutherfurd type ORDO:2709 SNOMEDCT:699754008 RGO:27318 Rutherfurd syndrome RGO:27318 RGO:27319 autosomal dominant absence of lower central incisor RGO:27319 ORDO:2899 RGO:27321 brachyolmia-like dysplasia with amelogenesis imperfecta RGO:27321 RGO:27322 branchiogenitoskeletal dysplasia RGO:27322 RGO:27323 cerebo-oculo-nasal syndrome RGO:27323 ORDO:99792 RGO:27324 dentine dysplasia-sclerotic bones RGO:27324 RGO:27325 distal symphalangism-dental syndrome RGO:27325 Heimler syndrome deafness - enamel hypoplasia - nail defects ORDO:3220 RGO:27327 enamel hypoplasia-hearing loss-nail defects RGO:27327 RGO:27330 Kohlschütter-Tönz syndrome RGO:27330 BMRS Ohdo type Ohdo-Madokoro-Sonoda syndrome blepharophimosis syndrome Ohdo type blepharophimosis-intellectual deficit syndrome Ohdo type DOID:0060289 ORDO:2728 RGO:27332 Ohdo syndrome RGO:27332 SNOMEDCT:389170006 RGO:27333 precocious osteodysplasty RGO:27333 ORDO:2916 RGO:27338 postaxial polydactyly-dental-vertebral syndrome RGO:27338 RGO:27339 radiculomegaly of canine teeth and congenital cataracts RGO:27339 ORDO:2036 RGO:27341 scalp-ear-nipple syndrome RGO:27341 RGO:27342 single central mandibular incisor RGO:27342 SMMCI single upper central incisor solitary median maxillary central incisor syndrome ORDO:2286 RGO:27343 single central maxillary incisor RGO:27343 RGO:27347 familial premature erupting teeth RGO:27347 ORDO:69082 RGO:27349 odonto-tricho-ungual-digital-palmar syndrome RGO:27349 epidermal polycystic disease sebocystomatosis HP:0012035 ICD10CM:L72.2 ORDO:3184 SNOMEDCT:109433009 RGO:27351 steatocystoma multiplex RGO:27351 RGO:27352 Riga-Fedes syndrome RGO:27352 RGO:27353 Walker-Warburg-like syndrome RGO:27353 RGO:27356 congenital nasal stenosis RGO:27356 RGO:27357 monosupero-centroincisodontic dwarfism RGO:27357 RGO:27358 ocular coloboma and single median incisor RGO:27358 RGO:27367 chromosome 22q11 syndrome RGO:27367 RGO:27368 dental noneruption RGO:27368 SNOMEDCT:38993008 RGO:27374 trichodento-osseous syndrome RGO:27374 diaphragmatic flutter moving umbilicus syndrome RGO:27376 belly-dancer dyskinesia RGO:27376 HP:0008986 RGO:27377 agenesis of the diaphragm RGO:27377 hypertrophic interstitial polyneuritis DOID:0050540 ORDO:64748 RGO:27378 Déjérine-Sottas syndrome RGO:27378 RGO:27382 familial congenital diaphragmatic defect RGO:27382 RGO:27384 neurogenic atrophy RGO:27384 RGO:27385 Parsonage-Turner syndrome RGO:27385 RGO:27387 Respiratory flutter syndrome RGO:27387 RGO:27388 thoracic insufficiency syndrome RGO:27388 RGO:27389 congenital unilateral hand muscular hyperplasia RGO:27389 RGO:27390 Hoffmann syndrome RGO:27390 DOID:7998 HP:0000836 RADLEX:RID45793 SNOMEDCT:34486009 RGO:27391 hyperthyroidism RGO:27391 DOID:14464 ORDO:94093 SNOMEDCT:15244003 RGO:27393 neuroleptic malignant syndrome RGO:27393 DOID:11726 ORDO:261 SNOMEDCT:111508004 RGO:27394 Emery-Dreifuss muscular dystrophy RGO:27394 RGO:27395 Fukuyama-type muscular dystrophy RGO:27395 ORDO:481 SNOMEDCT:230253001 RGO:27397 Kennedy syndrome RGO:27397 DOID:1440 RADLEX:RID5157 SNOMEDCT:91952008 RGO:27398 Machado-Joseph disease RGO:27398 RGO:27400 neurogenic scapuloperoneal amyotrophy RGO:27400 SNOMEDCT:278065000 RGO:27402 Pancoast syndrome RGO:27402 ORDO:2942 RGO:27403 post-polio syndrome RGO:27403 DOID:0050557 HP:0003741 ORDO:97242 SNOMEDCT:240059009 RGO:27406 congenital muscular dystrophy RGO:27406 ORDO:257 RGO:27410 epidermolysis bullosa simplex associated with muscular dystrophy RGO:27410 RGO:27411 hematuria-retinal arteriolar tortuosity-contractures RGO:27411 RGO:27413 lethal congenital muscular dystrophy with arthrogryposis multiplex congenita RGO:27413 RGO:27414 muscular dystrophy-rigid spine syndrome RGO:27414 RGO:27415 occidental congenital muscular dystropy RGO:27415 SNOMEDCT:4659007 RGO:27416 acne fulminans RGO:27416 RGO:27418 anti-Jo-1 antibody syndrome RGO:27418 SNOMEDCT:75659004 RGO:27420 Barraquer-Simons syndrome RGO:27420 RGO:27422 Calmette Guérin vaccination RGO:27422 adducted thumbs syndrome skeletal dysplasia - intellectual deficit RGO:27423 Christian syndrome RGO:27423 DOID:5212 SNOMEDCT:238049009 RGO:27425 carbohydrate-deficient glycoprotein syndrome RGO:27425 SNOMEDCT:449899001 RGO:27427 dropped head syndrome RGO:27427 RGO:27428 ethylmalonic-adipic aciduria RGO:27428 SNOMEDCT:396331005 RGO:27429 Gluten enteropathy RGO:27429 DOID:7188 HP:0000872 RADLEX:RID3669 SNOMEDCT:21983002 RGO:27431 Hashimoto thyroiditis RGO:27431 hyperglobulinemic purpura of Waldenström purpura hyperglobulinemica RGO:27432 Waldenström hyperglobulinemic purpura RGO:27432 RGO:27433 idiopathic inflammatory myopathy of the antisynthetase Jo-1 type RGO:27433 ORDO:611 RGO:27434 inclusion body myopathy RGO:27434 RGO:27435 infantile visceral myopathy RGO:27435 RADLEX:RID3710 SNOMEDCT:40733004 RGO:27436 infection RGO:27436 RGO:27437 King syndrome RGO:27437 DOID:13581 ICD10CM:E61.2 SNOMEDCT:238118002 RGO:27439 magnesium deficiency RGO:27439 SNOMEDCT:234411007 RGO:27440 McLeod syndrome RGO:27440 RADLEX:RID7478 RGO:27441 medication RGO:27441 RGO:27442 mitochondrial diabetes RGO:27442 DOID:699 HP:0003737 SNOMEDCT:16851005 RGO:27444 mitochondrial myopathy RGO:27444 DOID:0111040 ORDO:715 ORDO:79240 RGO:27445 muscle phosphorylase kinase deficiency RGO:27445 RGO:27446 myopathy-progeria syndrome RGO:27446 RGO:27450 progeria-myopathy syndrome RGO:27450 RGO:27451 Andersen syndrome RGO:27451 SNOMEDCT:20305008 RGO:27452 Becker myotonia congenita RGO:27452 HP:0100595 ORDO:1320 SNOMEDCT:13534001 RGO:27453 camptocormia RGO:27453 DOID:14451 HP:0007215 ORDO:682 SNOMEDCT:304737009 RGO:27454 hyperkalemic periodic paralysis RGO:27454 Thomsen disease DOID:2106 ICD10CM:G71.12 SNOMEDCT:57938005 RGO:27455 myotonia congenita RGO:27455 Steinert disease ICD10CM:G71.11 SNOMEDCT:77956009 RGO:27456 myotonic dystrophy RGO:27456 ORDO:684 SNOMEDCT:41574007 RGO:27457 paramyotonia congenita RGO:27457 myotonia fluctuans ORDO:612 RGO:27458 potassium-sensitive myotonia congenita RGO:27458 Aberfeld syndrome chondrodystrophic myotonia osteochondromuscular dystrophy ORDO:800 SNOMEDCT:29145002 RGO:27459 Schwartz-Jampel syndrome RGO:27459 RGO:27460 bilateral pectoralis muscle deficiency RGO:27460 RGO:27461 isolated pectoral muscle anomaly RGO:27461 ORDO:114 RGO:27462 auriculoosteodysplasia RGO:27462 HP:0009795 SNOMEDCT:204268008 RGO:27463 branchial cleft fistula RGO:27463 RGO:27465 branchial pit RGO:27465 SNOMEDCT:609143007 RGO:27467 Eagle syndrome RGO:27467 RGO:27468 hemangiomatous branchial cleft syndrome RGO:27468 DOID:12934 ICD10CM:H49.81 ORDO:480 SNOMEDCT:25792000 RGO:27469 Kearns-Sayre syndrome RGO:27469 RGO:27470 microtia-meatal atresia syndrome RGO:27470 SNOMEDCT:53103008 RGO:27473 cervical lymphadenectomy RGO:27473 familial cystic hygroma RGO:27478 familial nuchal bleb RGO:27478 RGO:27481 Golden-Lakim syndrome RGO:27481 RGO:27482 hemangiomatosis with hydrops fetalis and nuchal cystic hygroma RGO:27482 RGO:27484 Lenz microphthalmos syndrome RGO:27484 ORDO:295 RGO:27486 maternal parvovirus infection RGO:27486 RGO:27487 maternal smoking RGO:27487 RGO:27489 symphyseal spur RGO:27489 ORDO:839 RGO:27491 nephrotic syndrome Finnish type RGO:27491 RGO:27493 nuchal cyst-edema-cleft palate-short limb syndrome RGO:27493 RGO:27494 nuchal cystic hygroma-cleft palate RGO:27494 DOID:0060336 HP:0003535 ICD10CM:E71.111 SNOMEDCT:237950009 RGO:27498 3-methylglutaconic aciduria RGO:27498 RGO:27499 acalvaria with neurological abnormality RGO:27499 RGO:27500 amnion rupture sequence with exencephaly RGO:27500 DOID:0060668 HP:0002323 ICD10CM:Q00.0 SNOMEDCT:89369001 RGO:27501 anencephaly RGO:27501 absence of the telencephalon and diencephalon HP:0007268 SNOMEDCT:277922001 RGO:27503 aprosencephaly RGO:27503 SNOMEDCT:277921008 RGO:27505 atelencephaly RGO:27505 DOID:12849 HP:0000717 SNOMEDCT:408856003 RGO:27506 autism RGO:27506 RGO:27507 beta-hydroxyisobutyric aciduria RGO:27507 RGO:27508 brain dysgenesis-focal calcification RGO:27508 RGO:27509 brainstem dysgenesis-cranial nerve involvement RGO:27509 DOID:0060337 ORDO:66631 RGO:27510 CEDNIK syndrome RGO:27510 RGO:27512 chromosome abnormality RGO:27512 DOID:0060246 SNOMEDCT:716996008 RGO:27513 CRASH syndrome RGO:27513 RGO:27514 double cortex syndrome RGO:27514 RGO:27515 ectodermal dysplasia-cystic brain changes RGO:27515 ECCL Haberland syndrome ORDO:2396 SNOMEDCT:238905009 RGO:27516 encephalocraniocutaneous lipomatosis RGO:27516 RGO:27517 facial hemangioma-corticovascular dysplasia RGO:27517 RGO:27518 familial aplasia of the cerebellar vermis RGO:27518 RGO:27519 familial cerebellar hypoplasia and congenital lymphedema RGO:27519 RGO:27520 familial diffuse cortical dysplasia RGO:27520 ORDO:2048 RGO:27522 Foix-Chavany-Marie syndrome RGO:27522 RGO:27523 Fukuyama-type muscular RGO:27523 RGO:27527 hereditary nodular heterotopia and mega cisterna magna RGO:27527 RGO:27528 Larson-like syndrome RGO:27528 RGO:27531 nephronophthisis-encephalopathy RGO:27531 hemangiovascular complex RGO:27533 Pascual-Castroviejo syndrome RGO:27533 RGO:27534 perisylvian syndrome RGO:27534 DOID:906 RGO:27535 peroxisomal disorder RGO:27535 RGO:27536 polycystic brain and ectodermal dysplasia RGO:27536 DOID:3649 ORDO:765 SNOMEDCT:46683007 RGO:27540 pyruvate dehydrogenase deficiency RGO:27540 HP:0003643 ICD10CM:E72.19 ORDO:99731 SNOMEDCT:367368009 RGO:27543 sulfite oxidase deficiency RGO:27543 DOID:0050562 HP:0011097 ORDO:3451 SNOMEDCT:28055006 RGO:27545 West syndrome RGO:27545 RGO:27546 X-linked pachygyria and agenesis of the corpus callosum RGO:27546 DOID:11088 SNOMEDCT:413654009 RGO:27548 birth asphyxia RGO:27548 SNOMEDCT:405617006 RGO:27549 cardiovascular event RGO:27549 DOID:8659 RGO:27551 chickenpox RGO:27551 RGO:27552 complex neurologic syndrome-mitochondrial DNA mutation RGO:27552 RGO:27553 Coxsackie B virus infection RGO:27553 RGO:27555 Epstein-Barr virus infection RGO:27555 RGO:27556 familial hypocalcemia-hypocalciuria RGO:27556 DOID:0060800 ORDO:85335 RGO:27558 Fried syndrome RGO:27558 idiopathic lenticulodentate calcification RGO:27559 Hastings-James syndrome RGO:27559 DOID:12554 HP:0005575 ICD10CM:D59.3 ORDO:90038 RGO:27560 hemolytic-uremic syndrome RGO:27560 HP:0003128 SNOMEDCT:190882007 RGO:27562 lactic acidemia RGO:27562 RGO:27564 Measles encephalitis RGO:27564 RGO:27565 methemoglobinopathy RGO:27565 PKU DOID:9281 ORDO:716 ORDO:79254 SNOMEDCT:7573000 RGO:27569 phenylketonuria RGO:27569 RGO:27570 spondyloenchodrodysplasia RGO:27570 RGO:27572 leptomeningeal angiomatosis RGO:27572 RGO:27573 leukemia after intrathecal methotrexate RGO:27573 RGO:27574 ossifying meningoencephalitis RGO:27574 RGO:27575 purulent meningitis RGO:27575 RGO:27576 subarachnoid fat RGO:27576 ORDO:1229 RGO:27579 autosomal recessive congenital intrauterine infection-like syndrome RGO:27579 brain dysgenesis brain dysplasia HP:0002269 RGO:27580 neuronal migration disorder RGO:27580 RGO:27582 Breathnach syndrome RGO:27582 RGO:27584 cerebral calcification Kahn-Markowitz type RGO:27584 ORDO:313838 RGO:27586 Coats-plus syndrome RGO:27586 RGO:27588 Crome syndrome RGO:27588 RGO:27592 familial occipital calcification and epilepsy RGO:27592 RGO:27595 hypodipsic hypernatremia RGO:27595 RGO:27597 increased renal phosphate reabsorption RGO:27597 RGO:27605 meningioangiomatosis RGO:27605 DOID:890 SNOMEDCT:447292006 RGO:27609 mitochondrial encephalomyopathy RGO:27609 DOID:857 ICD10CM:D81.81 ORDO:148 SNOMEDCT:62151000119109 RGO:27610 multiple carboxylase deficiency RGO:27610 SNOMEDCT:208008 RGO:27612 neurocutaneous melanosis sequence RGO:27612 NF type 1 NF-1 NF1 type 1 neurofibromatosis von Recklinghausen disease DOID:8712 ORDO:636 RADLEX:RID34601 SNOMEDCT:92824003 RGO:27613 neurofibromatosis type 1 RGO:27613 NF type 2 NF-2 NF2 type 2 neurofibromatosis DOID:8712 ORDO:637 RADLEX:RID34602 SNOMEDCT:92503002 RGO:27614 neurofibromatosis type 2 RGO:27614 SNOMEDCT:408466002 RGO:27617 cardiac surgery RGO:27617 RGO:27618 Rambaud-Galian syndrome RGO:27618 RGO:27620 Tolmie syndrome RGO:27620 RGO:27621 Troost syndrome RGO:27621 RGO:27622 tubular stenosis dyplasia RGO:27622 RGO:27624 adenylosuccinase deficiency with cerebellar hypoplasia RGO:27624 RGO:27625 autosomal recessive cerebellar hypoplasia RGO:27625 RGO:27630 COACH syndrome new RGO:27630 RGO:27631 craniocerebellocardiac syndrome RGO:27631 RGO:27634 familial partial aplasia of the cerebellar vermis RGO:27634 DOID:4249 ORDO:356 SNOMEDCT:67155006 RGO:27635 Gerstmann-Sträussler-Scheinker syndrome RGO:27635 DOID:0060168 HP:0002927 SNOMEDCT:78311009 RGO:27636 histidinuria RGO:27636 RGO:27638 OFD-plus syndrome RGO:27638 SNOMEDCT:39640004 RGO:27640 Minamata disease RGO:27640 RGO:27641 molar tooth sign syndrome RGO:27641 RGO:27642 olivopontoneocerebellar hypoplasia/atrophy RGO:27642 DOID:0060264 RGO:27644 pontocerebellar hypoplasia RGO:27644 DOID:1089 HP:0010301 SNOMEDCT:249491000119100 RGO:27646 spinal dysraphism RGO:27646 endosteal sclerosis with cerebellar hypoplasia RGO:27647 Stoll-Charrow-Poznanski syndrome RGO:27647 RGO:27649 bilaterally absent carotid arteries with primitive transmaxillary arterial anastomosis RGO:27649 DOID:0060688 HP:0002408 ORDO:46724 SNOMEDCT:234142008 RGO:27650 cerebral arteriovenous malformation RGO:27650 RGO:27651 facial hemangioma and dilatation of the carotid siphon RGO:27651 RGO:27652 familial arteriovenous malformation RGO:27652 RGO:27653 familial cavernous angioma syndrome RGO:27653 RGO:27654 hereditary neurocutaneous angiomatosis RGO:27654 RGO:27661 PHACE association new RGO:27661 HP:0000113 RADLEX:RID34636 SNOMEDCT:82525005 RGO:27662 polycystic kidney disease RGO:27662 RGO:27663 telangiectasias RGO:27663 RADLEX:RID3365 SNOMEDCT:312946000 RGO:27664 Terson syndrome RGO:27664 RGO:27666 webbing of carotid and cerebral arteries RGO:27666 DOID:0060600 DOID:0090003 SNOMEDCT:702439002 RGO:27669 Andermann syndrome RGO:27669 RGO:27670 ARX mutation RGO:27670 HP:0011333 RGO:27671 asymmetric crying face syndrome RGO:27671 ORDO:1394 RGO:27672 cerebro-facio-thoracic dysplasia RGO:27672 RGO:27680 cryptorchidism and corpus callosum agenesis RGO:27680 RGO:27681 cutis tricolor syndrome RGO:27681 DOID:0090144 ORDO:2143 SNOMEDCT:702418009 RGO:27682 Donnai-Barrow syndrome RGO:27682 RGO:27684 familial agenesis of the corpus callosum and macrocephaly RGO:27684 RGO:27691 L1CAM gene abnormality RGO:27691 RGO:27692 Lennox Gastaut syndrome RGO:27692 RGO:27693 Lin-Gettig syndrome new RGO:27693 DOID:0060246 ORDO:2466 RGO:27694 MASA syndrome RGO:27694 RGO:27698 ocular albinism and hypoplastic corpus callosum RGO:27698 RGO:27701 disomy 15 syndrome RGO:27701 ORDO:1777 RGO:27702 Temtamy syndrome RGO:27702 RGO:27703 thrombocytopenia-absent corpus callosum syndrome RGO:27703 DK pho­comelia syndrome TAR-like syndrome von Voss-Cherstvoy syndrome ORDO:3439 RGO:27705 von Voss syndrome RGO:27705 RGO:27708 X-linked seizures - agenesis of corpus callosum - mental retardation RGO:27708 DOID:0050694 SNOMEDCT:699866005 RGO:27713 Brown-Vialetto-Van Laere syndrome RGO:27713 ICD10CM:G46.3 SNOMEDCT:87555007 RGO:27714 Claude syndrome RGO:27714 Miller-Fisher syndrome cranial variant of GBS cranial variant of Guillain-Barré syndrome ORDO:98919 SNOMEDCT:1767005 RGO:27716 Fisher syndrome RGO:27716 RGO:27717 Garcin syndrome RGO:27717 HP:0005890 RGO:27718 hyperostosis cranialis interna RGO:27718 SNOMEDCT:31382008 RGO:27720 jugular foramen syndrome RGO:27720 mental neuropathy SNOMEDCT:449769004 RGO:27722 numb chin syndrome RGO:27722 RADLEX:RID5360 SNOMEDCT:49783001 RGO:27723 paraneoplastic syndrome RGO:27723 RGO:27728 congenital fibrosis extraocular muscles-plus RGO:27728 RGO:27742 Hadju-Cheney syndrome RGO:27742 DOID:0050779 RGO:27743 hydrolethalus syndrome RGO:27743 RGO:27747 oculo-encephalo-hepato-renal syndrome RGO:27747 C syndrome RGO:27748 Opitz trigonocephaly syndrome RGO:27748 RGO:27749 pseudo-Meckel syndrome RGO:27749 DOID:0050560 ORDO:899 RGO:27750 Walker-Warburg syndrome RGO:27750 fetal warfarin syndrome RGO:27751 warfarin embryopathy RGO:27751 RGO:27752 XX-agonadism RGO:27752 SNOMEDCT:236546003 RGO:27753 aluminum intoxication RGO:27753 ORDO:363746 RGO:27754 Balint syndrome RGO:27754 DOID:0090129 SNOMEDCT:238001003 RGO:27756 carnitine palmitoyltransferase I deficiency RGO:27756 RGO:27759 congenital myoclonic encephalopathy RGO:27759 DOID:11949 ICD10CM:A81.0 ORDO:204 SNOMEDCT:792004 RGO:27760 Creutzfeldt-Jakob disease RGO:27760 RGO:27761 familial encephalopathy and L2-hydroxyglutaric aciduria RGO:27761 ORDO:25 SNOMEDCT:360416003 RGO:27762 glutaryl-CoA dehydrogenase deficiency RGO:27762 RGO:27764 heroin vapor toxic leukoencephalopathy RGO:27764 RGO:27765 hyperammonemic disorder RGO:27765 HP:0008358 SNOMEDCT:59655002 RGO:27766 hyperprolinemia RGO:27766 RGO:27767 intussusception encephalopathy RGO:27767 RGO:27768 Jansky-Bielschowsky disease RGO:27768 DOID:0050561 ICD10CM:G40.81 ORDO:2382 SNOMEDCT:230418006 RGO:27769 Lennox-Gastaut syndrome RGO:27769 ORDO:221074 SNOMEDCT:386766007 RGO:27770 Marchiafava-Bignami disease RGO:27770 RGO:27771 medium-chain acyl coenzyme A dehydrogenase deficiency RGO:27771 DOID:9268 HP:0008288 RGO:27773 nonketotic hyperglycinemia RGO:27773 ORDO:1183 SNOMEDCT:230350000 RGO:27774 opsoclonus-myoclonus syndrome RGO:27774 DOID:9271 ICD10CM:E72.4 ORDO:664 SNOMEDCT:80908008 RGO:27775 ornithine transcarbamylase deficiency RGO:27775 DOID:14701 ICD10CM:E71.121 ORDO:35 SNOMEDCT:69080001 RGO:27776 propionic acidemia RGO:27776 ICD10CM:I67.83 SNOMEDCT:450886002 RGO:27777 posterior reversible encephalopathy syndrome RGO:27777 ORDO:3006 RGO:27778 pyridoxine-dependent seizures RGO:27778 ORDO:3008 SNOMEDCT:87694001 RGO:27779 pyruvate carboxylase deficiency RGO:27779 Rasmussen subacute encephalitis ORDO:1929 SNOMEDCT:230191005 RGO:27780 Rasmussen syndrome RGO:27780 RGO:27781 superficial siderosis of the central nervous system RGO:27781 ORDO:306731 RGO:27783 Sydenham chorea RGO:27783 RGO:27784 valproic acid-induced hyperammonemic encephalopathy RGO:27784 DOID:0050731 DOID:8459 HP:0100502 ICD10CM:E53.8 SNOMEDCT:190634004 RGO:27785 vitamin B12 deficiency RGO:27785 DOID:10915 SNOMEDCT:69482004 RGO:27786 Wernicke-Korsakoff syndrome RGO:27786 RGO:27789 autosomal recessive hydrocephalus RGO:27789 ORDO:156731 RGO:27792 dyssegmental dysplasia Rolland-Desbuquois type RGO:27792 RGO:27794 familial renal-hepatic-pancreatic dysplasia and Dandy-Walker cyst RGO:27794 RGO:27795 Hakim syndrome RGO:27795 RGO:27796 familial hydrocephalus RGO:27796 dysmorphism-holoprosencephaly sequence RGO:27805 hamartoblastoma and locoregional anomaly RGO:27805 RGO:27806 hamartoblastoma-frontonasal dysplasia syndrome RGO:27806 RGO:27807 isolated hamartoblastoma RGO:27807 DOID:10588 SNOMEDCT:65389002 RGO:27809 adrenoleukodystrophy RGO:27809 RGO:27810 bone marrow transplantation leukodystrophy RGO:27810 Cree leukoencephalopathy ORDO:99854 RGO:27811 Cree encephalopathy RGO:27811 HP:0003150 SNOMEDCT:28987007 RGO:27812 glutaric aciduria RGO:27812 RGO:27814 megancephalic leukoencephalopathy RGO:27814 Navajo neurohepatopathy ORDO:255229 RGO:27816 Navajo neuropathy RGO:27816 Sudanophilic leukodystrophy RGO:27817 orthochromatic leukodystrophy RGO:27817 SNOMEDCT:67434000 RGO:27819 cytochrome c oxidase deficiency RGO:27819 SNOMEDCT:237983002 RGO:27820 fumarase deficiency RGO:27820 RGO:27823 sequelae of boxing RGO:27823 RGO:27825 cerebrofaciothoracic syndrome RGO:27825 RGO:27826 chromosome 22q11 deletion RGO:27826 Tourette syndrome RGO:27827 Gilles de la Tourette syndrome RGO:27827 SNOMEDCT:71779008 RGO:27832 X-linked hydrocephalus RGO:27832 DOID:2810 SNOMEDCT:28295001 RGO:27834 middle lobe syndrome RGO:27834 RGO:27837 cardiac defects - laryngeal anomalies - polydactyly - colonic aganglionosis RGO:27837 CHAOS RGO:27838 congenital high airway obstruction syndrome RGO:27838 RGO:27841 irritable larynx syndrome RGO:27841 RGO:27842 laryngeal-tracheal agenesis RGO:27842 RGO:27843 laryngotracheoesophageal cleft RGO:27843 familial spontaneous pneumothorax ORDO:2903 RGO:27850 familial primary spontaneous pneumothorax RGO:27850 DOID:0050811 DOID:12255 HP:0008258 ICD10CM:E25.0 ORDO:418 SNOMEDCT:237751000 RGO:27861 congenital adrenal hyperplasia RGO:27861 chondrodysplasia punctata Curry type RGO:27864 chondrodysplasia punctata X-linked recessive type RGO:27864 RGO:27866 lethal skeletal dysplasias RGO:27866 ORDO:3348 RGO:27867 tracheobronchopathia osteochondroplastica RGO:27867 TE fistula TEF tracheo-esophageal fistula HP:0002575 RADLEX:RID4859 SNOMEDCT:95435007 RGO:27873 tracheoesophageal fistula RGO:27873 HP:0010450 RGO:27875 esophageal stenosis RGO:27875 RGO:27876 familial esophageal atresia-tracheoesophageal fistula RGO:27876 maternal hyperthyroidism RGO:27877 infant of hyperthyroid mother RGO:27877 RGO:27880 Rett syndrome-plus RGO:27880 RGO:27881 tracheoesophageal fistula-gastrointestinal abnormality-hypospadias-growth deficiency RGO:27881 RGO:27885 acroosteolysis-proximal symphangilism RGO:27885 RGO:27886 Bureau-Barriere syndrome RGO:27886 RGO:27887 familial neurogenic acroosteolysis RGO:27887 RGO:27889 idiopathic phalangeal acroosteolysis RGO:27889 RGO:27894 Cochin Jewish disorder RGO:27894 ORDO:3130 RGO:27895 Satoyoshi syndrome RGO:27895 RGO:27897 vinyl chloride exposure RGO:27897 Adducted Thumb-Clubfoot syndrome RGO:27898 adducted thumbs-clubfoot syndrome RGO:27898 RGO:27901 familial arachnodactyly-distal arthrogryposis RGO:27901 DOID:0060364 ORDO:2065 RGO:27902 Galloway-Mowat syndrome RGO:27902 ORDO:2342 RGO:27903 Haim-Munk syndrome RGO:27903 RGO:27905 Marfan-like syndrome with spastic paraparesis RGO:27905 BLC Blomstrand lethal chondrodysplasia chondrodysplasia Blomstrand type ORDO:50945 SNOMEDCT:389237009 RGO:27908 Blomstrand dysplasia RGO:27908 RGO:27913 distal osteosclerosis RGO:27913 congenital bowing of long bones ORDO:2292 RGO:27914 familial congenital bowing of the long bones RGO:27914 ORDO:1118 RGO:27916 fibular aplasia-ectrodactyly RGO:27916 DOID:0090067 ORDO:2854 RGO:27919 Fuhrmann syndrome RGO:27919 RGO:27921 Koller syndrome RGO:27921 RGO:27923 metaphyseal chondrodysplasia McKusick type RGO:27923 metaphyseal dysplasia Schmid type ORDO:174 RGO:27924 metaphyseal chondrodysplasia Schmid type RGO:27924 RGO:27926 ophthalmo-mandibulo-melic dysplasia RGO:27926 RGO:27928 pachydysostosis of the fibula RGO:27928 RGO:27929 physiologic bowing of infancy RGO:27929 RGO:27930 Pointer syndrome RGO:27930 RGO:27932 serpentine fibula-polycystic kidney syndrome RGO:27932 RGO:27933 skeletal dysplasia-pursed lips-ectopia lentis RGO:27933 RGO:27935 fibrocartilaginous dysplasia RGO:27935 DOID:0050604 ORDO:63446 RGO:27937 acrocapitofemoral dysplasia RGO:27937 RGO:27938 acrodysostosis and protrusio acetabuli RGO:27938 acromesomelic dysplasia with genital anomalies RGO:27941 acromesomelic dysplasia-genital anomaly RGO:27941 Dieker-Opitz syndrome DOID:0060347 ORDO:971 RGO:27942 acrorenal syndrome RGO:27942 SNOMEDCT:389162001 RGO:27943 acroscyphodysplasia RGO:27943 ORDO:63442 RGO:27944 angel-shaped phalango-epiphyseal dysplasia RGO:27944 RGO:27945 autosomal recessive short-limb dwarfism, absent fibulae, and brachydactyly RGO:27945 RGO:27946 baby-rattle pelvis dysplasia RGO:27946 RGO:27948 brachydactylic multiple delta phalanges plus syndrome RGO:27948 RGO:27949 brachydactyly E-plus syndrome RGO:27949 RGO:27953 brachydactyly-nail dysplasia RGO:27953 RGO:27963 cheirolumbar dysostosis RGO:27963 RGO:27964 Christian spondylo-digital syndrome RGO:27964 RGO:27966 congenital dyserythropoietic anemia-plus RGO:27966 Tonoki-Ohura-Niikawa syndrome cryptomicrotia - brachydactyly - excess fingertip arch ORDO:1547 RGO:27968 cryptomicrotia-brachydactyly syndrome RGO:27968 Eiken syndrome ORDO:79106 RGO:27970 Eiken dysplasia RGO:27970 RGO:27971 faciothoracoskeletal syndrome RGO:27971 RGO:27976 familial brachydactyly RGO:27976 RGO:27980 Fitzsimmons syndrome RGO:27980 RGO:27981 Frias syndrome RGO:27981 ORDO:85201 SNOMEDCT:702367005 RGO:27982 genitopatellar syndrome RGO:27982 RGO:27983 GOMBO syndrome RGO:27983 ORDO:79094 RGO:27984 Grange syndrome RGO:27984 hand-heart syndrome DOID:0060468 RGO:27986 heart-hand syndrome RGO:27986 DOID:12466 HP:0000867 SNOMEDCT:91478007 RGO:27989 secondary hyperparathyroidism RGO:27989 RGO:27992 Iso-Kikuchi syndrome plus RGO:27992 RGO:27993 Liebenberg syndrome RGO:27993 RGO:27999 mitral valve insufficiency-deafness-skeletal malformation RGO:27999 SNOMEDCT:401046009 RGO:28005 Nicolaides-Baraitser syndrome RGO:28005 RGO:28008 osteosclerosis dominant type RGO:28008 ORDO:90650 RGO:28009 otopalatodigital syndrome type 1 RGO:28009 ORDO:90652 SNOMEDCT:42432003 RGO:28010 otopalatodigital syndrome type 2 RGO:28010 rhizomelic dysplasia Patterson-Lowry type ORDO:2831 RGO:28011 Patterson-Lowry rhizomelic dysplasia RGO:28011 Krause-Kivlin syndrome Krause-van Schooneveld-Kivlin syndrome DOID:0080201 ORDO:709 RGO:28012 Peters-plus syndrome RGO:28012 RGO:28013 Senior-Loken syndrome plus RGO:28013 RGO:28017 short stature, contractures, upper body pterygia, brachydactyly RGO:28017 RGO:28018 spondyloepimetaphyseal dysplasia cone-shaped epiphysis type RGO:28018 RGO:28019 spondyloepimetaphyseal dysplasia dominant metatropic type RGO:28019 ORDO:93351 SNOMEDCT:717330004 RGO:28020 spondyloepimetaphyseal dysplasia Irapa type RGO:28020 RGO:28023 symbrachydactyly-oligodactyly RGO:28023 RGO:28024 synpolydactyly-brachydactyly RGO:28024 RGO:28025 Tabatznik syndrome RGO:28025 RGO:28028 Tonoki syndrome RGO:28028 ORDO:52056 RGO:28029 ulnar/fibular ray defect-brachydactyly RGO:28029 Ghosal hematodiaphyseal dysplasia hematodyaphyseal dysplasia Ghosal type RGO:28031 diaphyseal dysplasia Ghosal hemato type RGO:28031 RGO:28032 diaphyseal dysplasia-proximal myopathy RGO:28032 RGO:28033 Léri syndrome RGO:28033 RGO:28037 rhizomelic bone dysplasia RGO:28037 RGO:28039 ankle-foot coalition RGO:28039 DOID:0090127 ORDO:2848 RGO:28041 camptodactyly-arthropathy-coxa vara-pericarditis syndrome RGO:28041 RGO:28043 camptodactyly-ichthyosis syndrome RGO:28043 DOID:0060294 ORDO:1545 SNOMEDCT:702363009 RGO:28045 Crisponi syndrome RGO:28045 RGO:28047 familial camptodactyly RGO:28047 RGO:28048 familial camptodactylyscoliosis RGO:28048 ORDO:1327 RGO:28051 Guadalajara camptodactyly type 1 RGO:28051 ORDO:1326 RGO:28052 Guadalajara camptodactyly type 2 RGO:28052 RGO:28057 Stewart-Bergstrom syndrome RGO:28057 ORDO:3291 RGO:28058 Teebi-Shaltout syndrome RGO:28058 ORDO:3377 RGO:28059 trismus-pseudocamptodactyly syndrome RGO:28059 RGO:28061 carpal coalition-plus RGO:28061 RGO:28063 dislocated hips and radial heads - carpal coalition - short stature RGO:28063 RGO:28065 Du Pan-like syndrome with genital anomalies RGO:28065 RGO:28067 mitral valve insufficiency-deafness-skeletal malformation syndrome RGO:28067 RGO:28069 Osebold-Remondini dysplasia RGO:28069 RGO:28072 split hand and foot RGO:28072 RGO:28073 symphalangism complete-carpal fusion RGO:28073 Keipert syndrome RGO:28079 nasodigitoacoustic syndrome RGO:28079 RGO:28082 familial clubbed fingers RGO:28082 RGO:28089 pulmonary tumor RGO:28089 DOID:0080194 ORDO:1358 RGO:28092 Carey-Fineman-Ziter syndrome RGO:28092 RGO:28093 clubfeet and tarsal coalition RGO:28093 RGO:28096 idiopathic talipes equinovarus RGO:28096 RGO:28099 SAMS syndrome RGO:28099 SNOMEDCT:715440003 RGO:28100 Sandrow syndrome RGO:28100 RGO:28102 Caffey dysplasia RGO:28102 RGO:28104 diaphyseal dysplasia and proximal myopathy RGO:28104 RGO:28106 endosteal hyperostosis van Buchem type RGO:28106 ORDO:53697 SNOMEDCT:715568002 RGO:28107 gnathodiaphyseal dysplasia RGO:28107 RGO:28108 Goldbloom syndrome RGO:28108 RGO:28109 Kozlowski-Tsuruta syndrome RGO:28109 RGO:28111 normal neonatal cortical hyperostosis RGO:28111 RGO:28113 pamidronate therapy RGO:28113 RGO:28119 metaphyseal-sella turcica dysplasia-Rosenberg RGO:28119 SNOMEDCT:257277002 RGO:28121 neuromuscular disorder RGO:28121 RGO:28123 spondyloepiphyseal dysplasia Stanescu type RGO:28123 Ollier disease DOID:4625 ICD10CM:Q78.4 ORDO:296 RADLEX:RID4129 SNOMEDCT:268274005 RGO:28126 enchondromatosis RGO:28126 RGO:28129 FGFR-opathy RGO:28129 ORDO:1824 RGO:28131 Lowry-Wood syndrome RGO:28131 MOPD osteodysplastic primordial dwarfism RGO:28133 microcephalic osteodysplastic primordial dwarfism RGO:28133 RGO:28134 nondevelopmental dysplasia of the hips RGO:28134 RGO:28135 patella aplasia-coxa vara-tarsal synostosis RGO:28135 RGO:28137 rhizomelic limb dwarfism and cataracts RGO:28137 ORDO:93315 RGO:28138 spondylometaphyseal dysplasia corner-fracture type RGO:28138 RGO:28140 tibial-femoral hypoplasia with hook pelvis RGO:28140 Horn-Kolb syndrome acheiropody aleijadinhos Brazilian type DOID:0050603 ORDO:931 SNOMEDCT:177504007 RGO:28148 acheiropodia RGO:28148 RGO:28149 anonychia-ectrodactyly syndrome RGO:28149 RGO:28152 chorionic villus sampling-transverse limb deficiency RGO:28152 ORDO:2019 RGO:28158 femur-fibula-ulna syndrome RGO:28158 RGO:28159 fetal phenytoin toxicity RGO:28159 RGO:28160 fetal pyrimethamine syndrome RGO:28160 RGO:28161 humeroradioulnar synostosis and oligoectrosyndactyly RGO:28161 RGO:28163 Marles-Chudley syndrome RGO:28163 polyoligodactyly-imperforate anus-vertebral anomaly syndrome RGO:28168 PIV syndrome RGO:28168 RGO:28170 split-hand split-foot deformity RGO:28170 RGO:28173 ulnar aplasia with foot ectrodactyly RGO:28173 RGO:28178 disorganization complex RGO:28178 RGO:28179 femoral duplication RGO:28179 RGO:28180 fibular dimelia and tibial deficiency RGO:28180 fibular dimelia - diplopodia ORDO:1757 RGO:28182 fibular dimelia and duplicated foot RGO:28182 humero-spinal dysostosis DOID:0050813 RGO:28183 humerospinal dysostosis RGO:28183 RGO:28184 limb duplication-renal agenesis syndrome RGO:28184 RGO:28189 supernumerary limbs-plus RGO:28189 RGO:28195 ankyloglossia superior RGO:28195 RGO:28198 chorionic villus sampling RGO:28198 RGO:28199 chromosome 7q abnormality RGO:28199 RGO:28200 ectromelia associated with interstitial deletion of 7q RGO:28200 RGO:28204 ectrodactyly and cleft palate syndrome RGO:28204 RGO:28206 familial split hand-split foot anomaly RGO:28206 RGO:28207 fetal alcohol exposure RGO:28207 RGO:28209 Ives-Houston syndrome RGO:28209 ORDO:69085 RGO:28211 limb-mammary syndrome RGO:28211 RGO:28213 Scalp defects and ectrodactyly RGO:28213 ORDO:3329 RGO:28216 tibial agenesis-ectrodactyly syndrome RGO:28216 RGO:28219 auriculo-osteodysplasia RGO:28219 RGO:28221 diabetic fetopathy RGO:28221 RGO:28223 familial dislocation of radial head RGO:28223 RGO:28226 metatropic dysplasia variant RGO:28226 MOPD type 2 MOPD2 osteodysplastic primordial dwarfism type 2 ORDO:2637 RGO:28227 microcephalic osteodysplastic primordial dwarfism type 2 RGO:28227 RGO:28231 anorchia and cone-shaped epiphyses RGO:28231 RGO:28240 trichoscyphodysplasia RGO:28240 ORDO:99645 SNOMEDCT:389262009 RGO:28245 dappled diaphyseal dysplasia RGO:28245 RGO:28251 Smith-Lemli-Opitz syndrome type 1 RGO:28251 RGO:28252 spondyloepimetaphyseal dysplasia leptodactylic type RGO:28252 RGO:28253 spondyloepimetaphyseal dysplasia short limb-hand-abnormal calcification type RGO:28253 SNOMEDCT:35908007 RGO:28255 chronic arthritis RGO:28255 SNOMEDCT:125163009 RGO:28256 healing fracture RGO:28256 RGO:28259 megaepiphyseal dysplasia RGO:28259 metaphyseal dysplasia-microspherophakia ORDO:2551 RGO:28260 microspherophakia-metaphyseal dysplasia RGO:28260 RGO:28261 idiopathic precocious puberty RGO:28261 RGO:28265 estrogen deficiency in males RGO:28265 RGO:28266 irritable hip syndrome RGO:28266 RGO:28269 septic joint RGO:28269 RGO:28270 slipped epiphysis RGO:28270 RGO:28271 vasculopathy RGO:28271 RGO:28282 multicentric fibromatosis with metaphyseal dysplasia RGO:28282 BFHD Beukes familial hip dysplasia familial hip dysplasia ORDO:2114 RGO:28283 autosomal dominant premature degenerative osteoarthropathy of the hip RGO:28283 MEN 2B ORDO:247709 RGO:28287 multiple endocrine neoplasia syndrome type 2B RGO:28287 adiposogenital syndrome RGO:28291 Fröhlich syndrome RGO:28291 RGO:28293 hemosiderosis-panhypopituitarism RGO:28293 RGO:28294 hypoestrogenic state RGO:28294 RGO:28295 idiopathic slipped capital femoral epiphysis RGO:28295 DOID:9410 HP:0000871 ICD10CM:E23.0 ORDO:90695 SNOMEDCT:32390006 RGO:28296 panhypopituitarism RGO:28296 RGO:28297 peroneal spastic flatfoot with slipped femoral head RGO:28297 SNOMEDCT:127024001 RGO:28298 pituitary tumor RGO:28298 RGO:28299 familial congenital bowing RGO:28299 SNOMEDCT:205473008 RGO:28302 mesomelic dysplasia RGO:28302 RGO:28303 physiologic femoral bowing RGO:28303 RGO:28309 absent fibula-craniosynostosis RGO:28309 RGO:28311 bilateral congenital transverse deficiency of the tibia and fibula RGO:28311 RGO:28314 discordant fibular aplasia RGO:28314 ORDO:93323 RGO:28315 fibular hemimelia RGO:28315 fibulo-ulnar hypoplasia - renal anomalies ORDO:2256 RGO:28317 fibuloulnar aplasia/hypoplasia and renal dysplasia RGO:28317 mesomelic dysplasia Kantaputra type ORDO:1836 RGO:28318 Kantaputra mesomelic dysplasia RGO:28318 RGO:28319 limb deficiency-heart malformation syndrome RGO:28319 RGO:28320 mesomelic dysplasia-absent fibulae-triangular tibiae RGO:28320 RGO:28322 orofaciodigital syndrome plus RGO:28322 RGO:28323 osteofibrous dysplasia-fibular pseudoarthrosis RGO:28323 RGO:28324 otoonychoperoneal syndrome RGO:28324 RGO:28325 ulna-fibula deficiency RGO:28325 RGO:28328 hereditary pubertal genu valgum RGO:28328 RGO:28329 postinflammatory deformity RGO:28329 RGO:28330 posttraumatic deformity RGO:28330 HP:0100694 SNOMEDCT:249785006 RGO:28333 tibial torsion RGO:28333 RGO:28334 chromosome 11p- syndrome RGO:28334 HP:0100777 RGO:28335 exostoses RGO:28335 RGO:28337 oculo-palatal-cerebral syndrome RGO:28337 RGO:28340 dystonic clenched fist RGO:28340 RGO:28343 windblown hand deformity RGO:28343 RGO:28344 Carnevale syndrome RGO:28344 ORDO:1508 RGO:28345 coxoauricular syndrome RGO:28345 RGO:28346 Farber syndrome RGO:28346 RGO:28347 habitual hip dislocation RGO:28347 DOID:870 HP:0009830 RADLEX:RID29115 SNOMEDCT:386033004 RGO:28348 neuropathy RGO:28348 RGO:28350 voluntary habitual dislocation RGO:28350 RGO:28353 Desbuquios dysplasia RGO:28353 RGO:28359 congenital sensory neuropathy and anhidrosis RGO:28359 brachydactylous dwarfism Mseleni type brachydactylous dwarfism of Mseleni ORDO:2619 SNOMEDCT:715470008 RGO:28360 Mseleni joint disease RGO:28360 RGO:28362 spondyloepiphyseal tarda RGO:28362 SNOMEDCT:77016009 RGO:28364 amyoplasia congenita RGO:28364 ORDO:2962 SNOMEDCT:238826008 RGO:28366 de Barsy syndrome RGO:28366 RGO:28367 familial subluxation of the metacarpophalangeal and proximal interphalangeal joints of the little finger RGO:28367 RGO:28373 genito-patellar syndrome RGO:28373 Giedion syndrome TRPS1 trichorhinophalangeal syndrome type 1 RGO:28386 trichorhinophalangeal dysplasia type 1 RGO:28386 RGO:28387 voluntary subluxation of the shoulder RGO:28387 DOID:14775 ORDO:90354 RGO:28390 brittle cornea syndrome RGO:28390 RGO:28391 cerebrofacioauricular syndrome of Van Maldergem RGO:28391 RGO:28392 chromosome 6q deletion RGO:28392 RGO:28393 deafness and metaphyseal dysostosis RGO:28393 DOID:13781 ICD10CM:M35.7 SNOMEDCT:85551004 RGO:28397 hypermobility syndrome RGO:28397 RGO:28398 joint laxity-idiopathic scoliosis RGO:28398 RGO:28403 osteoma cutis with dysmorphism RGO:28403 Pashayan syndrome blepharonasofacial malformation syndrome RGO:28404 Pashayan-Pruzansky syndrome RGO:28404 spondylometaphyseal dysplasia with joint laxity and dentinogenesis imperfecta ORDO:166272 RGO:28406 Goldblatt syndrome RGO:28406 DOID:0050631 ORDO:59 SNOMEDCT:702327009 RGO:28407 Allan-Herndon-Dudley syndrome RGO:28407 RGO:28408 ankylosed thumbs and mental retardation RGO:28408 RGO:28410 bee-keeper arthropathy RGO:28410 ORDO:2767 SNOMEDCT:389272007 RGO:28411 carpotarsal osteochondromatosis RGO:28411 RGO:28416 Debuquois dysplasia RGO:28416 ORDO:1927 RGO:28418 Emery-Nelson syndrome RGO:28418 glaucoma-ectopia lentis-microspherophakia-stiff joint-short stature syndrome DOID:0050475 RGO:28419 GEMSS syndrome RGO:28419 RGO:28420 Nevo syndrome RGO:28420 pelvic dysplasia - arthrogryposis of lower limbs pelvic dysplasia - lower limb arthrogryposis ORDO:2840 RGO:28422 pelvic dysplasia - arthrogrypotic lower limbs RGO:28422 turned head-adducted hip-truncal curvature syndrome RGO:28426 TAC syndrome RGO:28426 ORDO:2460 RGO:28427 van den Ende-Gupta syndrome RGO:28427 RGO:28428 X-linked mental retardation with clasped thumbs RGO:28428 RGO:28432 cavernous angiomatosis and forearm transverse defect RGO:28432 RGO:28434 diaphragmatic hernia and ipsilateral upper limb reduction RGO:28434 RGO:28439 limb reduction defect and renal dysplasia RGO:28439 RGO:28443 microgastria and limb reduction defects RGO:28443 DOID:0060055 SNOMEDCT:66783006 RGO:28445 popliteal pterygium syndrome RGO:28445 SNOMEDCT:715522000 RGO:28446 Schinzel phocomelia syndrome RGO:28446 tetra-amelia ORDO:3301 RGO:28448 familial tetra-amelia and multiple malformations RGO:28448 RGO:28449 urethral obstruction sequence and lower limb deficiency RGO:28449 RGO:28451 digital deficiency RGO:28451 RGO:28452 intercalary limb reduction RGO:28452 absence or severe hypoplasia of the postaxial structures RGO:28453 longitudinal postaxial limb reduction RGO:28453 absence or severe hypoplasia of the preaxial structures RGO:28454 longitudinal preaxial limb reduction RGO:28454 RGO:28455 mixed-type limb reduction RGO:28455 hypoplasia of all skeletal structures of a limb RGO:28456 rudimentary limb RGO:28456 absence or severe hypoplasia of the central axis, normal or near-normal lateral digits RGO:28457 split type limb reduction RGO:28457 absence or severe hypoplasia of distal segment of a limb RGO:28458 transverse limb reduction RGO:28458 RGO:28463 giant cell tumor of the tendon sheath RGO:28463 RGO:28475 Hardcastle syndrome RGO:28475 HP:0003797 RGO:28476 Limb-girdle myopathy RGO:28476 RGO:28477 Tubular stenosis RGO:28477 atelosteogenesis 2-like RGO:28478 atelosteogenesis type 2-like RGO:28478 RGO:28479 brachymesomelia and Peters anomaly RGO:28479 RGO:28483 mesomelic dysplasia with spur-limbs RGO:28483 ORDO:1865 RGO:28485 dyssegmental dysplasia Silverman-Handmaker type RGO:28485 SNOMEDCT:77542002 RGO:28486 Grebe dysplasia RGO:28486 DOID:0060467 HP:0003041 SNOMEDCT:205329008 RGO:28487 humeroradial synostosis RGO:28487 SNOMEDCT:66651005 RGO:28489 triploidy syndrome RGO:28489 brachydactyly Farabee type DOID:0110964 ORDO:93388 SNOMEDCT:715720006 RGO:28492 brachydactyly type A1 RGO:28492 ORDO:93387 RGO:28493 brachydactyly type E RGO:28493 RGO:28495 chromosome 5p partial deletion RGO:28495 RGO:28496 Devriendt syndrome RGO:28496 RGO:28497 dyssegmental dwarfism RGO:28497 ORDO:2026 RGO:28499 hypertrichosis-gingival fibromatosis-mental retardation syndrome RGO:28499 ORDO:66518 RGO:28500 insulin resistance-short fifth metacarpal syndrome RGO:28500 RGO:28501 metacarpal 4-5 synostosis RGO:28501 RGO:28503 oto-palato-digital syndrome type 1 RGO:28503 RGO:28504 oto-palato-digital syndrome type 2 RGO:28504 ORDO:1240 RGO:28507 metaphyseal acroscyphodysplasia RGO:28507 RGO:28508 metaphyseal-sella turcica dysplasia Rosenberg type RGO:28508 short rib-polydactyly syndrome Verma-Naumoff type RGO:28513 short rib-polydactyly syndrome type 3 RGO:28513 RGO:28516 bisphosphonate therapy RGO:28516 RGO:28518 deferoxamine-induced skeletal dysplasia RGO:28518 RGO:28519 fetal hypermagnesemia syndrome RGO:28519 RGO:28520 idiopathic symptomatic metaphyseal sclerosis in children RGO:28520 RGO:28523 Plasma-cell osteomyelitis RGO:28523 RGO:28524 round distal femoral epiphyseal micromelic dysplasia RGO:28524 RGO:28531 familial overgrowth RGO:28531 RGO:28532 hypertrichotic osteochondrodysplasia RGO:28532 RGO:28537 spondyloepimetaphyseal dysplasia Maroteaux type RGO:28537 Biemond syndrome 1 RGO:28539 Biemond syndrome type 1 RGO:28539 mosaic trisomy 9 RGO:28541 chromosome 9 mosaic trisomy syndrome RGO:28541 DOID:0060732 RGO:28542 chromosome 9p syndrome RGO:28542 RGO:28544 Grebe chondrodystrophy RGO:28544 ORDO:295036 RGO:28546 congenital patella dislocation RGO:28546 RGO:28550 familial dislocation of patellae RGO:28550 RGO:28553 ischio-patellar dysplasia RGO:28553 RGO:28558 patella infra RGO:28558 galactosialidosis infantile form RGO:28563 galactosialidosis variant RGO:28563 RGO:28564 osteogenesis imperfecta-like syndrome RGO:28564 RGO:28567 crossed polydactyly RGO:28567 ORDO:93338 SNOMEDCT:84598000 RGO:28568 polysyndactyly RGO:28568 RGO:28570 bifid epiglottis-polydactyly syndrome RGO:28570 RGO:28571 cerebrorenodigital syndrome RGO:28571 RGO:28573 cutis tricolor neurocutaneous malformation syndrome RGO:28573 ORDO:2935 RGO:28575 familial crossed polysyndactyly RGO:28575 RGO:28577 hepatic fibrocystic disease and polydactyly RGO:28577 ORDO:3332 RGO:28580 hypoplastic tibiae and postaxial polysyndactyly RGO:28580 RGO:28582 myopia-polydactyly RGO:28582 RGO:28590 tetrapolysyndactyly and postaxial polydactyly RGO:28590 RGO:28596 familial preaxial polydactyly RGO:28596 RGO:28599 Laurin-Sandrow syndrome 2 RGO:28599 RGO:28601 postaxial dysostosis Arens type RGO:28601 acrofacial dysostosis Rodriguez type RGO:28602 Rodriquez acrofacial dysostosis syndrome RGO:28602 ORDO:66630 RGO:28607 familial pseudoarthrosis of the clavicle RGO:28607 pseudoarthrosis of the talus RGO:28608 posterior ankle impingement syndrome RGO:28608 RGO:28609 posttraumatic pseudoarthrosis RGO:28609 ORDO:357131 SNOMEDCT:25981000119102 RGO:28610 venous thoracic outlet syndrome RGO:28610 ORDO:3016 RGO:28611 absent radius and anogenital anomaly RGO:28611 RGO:28613 autosomal dominant congenital erythroid hypoplastic anemia and radial ray abnormality RGO:28613 RGO:28619 fetal valproic acid exposure RGO:28619 RGO:28621 isolated radial deficiency RGO:28621 RGO:28623 limb/pelvis hypoplasia/aplasia-like syndrome RGO:28623 Mayer-Rokitansky-Küster syndrome ORDO:247775 ORDO:3109 RGO:28624 Mayer-Rokitansky-Küster-Hauser syndrome RGO:28624 RGO:28627 pulmonary agenesis-radial ray association RGO:28627 ORDO:1121 RGO:28628 radial deficiency with lower limb deficiency RGO:28628 ORDO:2252 RGO:28629 radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema RGO:28629 RGO:28634 radiodigitofacial dysplasia RGO:28634 RGO:28635 radioulnar synostosis and radial ray defect RGO:28635 ORDO:3466 RGO:28637 WT limb-blood syndrome RGO:28637 RGO:28638 femoral dysplasia RGO:28638 RGO:28641 metaphyseal chondrodysplasia anadysplasia type RGO:28641 RGO:28642 micromelic dwarfism humerus-femur-tibia type RGO:28642 RGO:28647 spondyloepiphyseal dysplasia Omani type RGO:28647 RGO:28649 gracile bone dysplasia group RGO:28649 RGO:28651 microcephalicosteodysplastic primordial dwarfism RGO:28651 RADLEX:RID49606 RGO:28652 muscular disorder RGO:28652 TORCH complex RGO:28657 congenital transplacental infection RGO:28657 RGO:28658 lipodystrophy Rajab type RGO:28658 RGO:28661 rapid demineralization RGO:28661 ORDO:93383 RGO:28662 brachydactyly type B RGO:28662 ORDO:3248 RGO:28663 familial distal symphalangism RGO:28663 RGO:28664 hereditary symphalangism and tarsal synostosis RGO:28664 brachydactyly Mohr-Wriedt type DOID:0110965 ORDO:93396 RGO:28667 brachydactyly type A2 RGO:28667 ORDO:806 RGO:28669 craniodigital syndrome of Scott RGO:28669 RGO:28674 familial syndactyly with metacarpal and metatarsal fusion RGO:28674 heart-hand syndrome Spanish type ORDO:1342 RGO:28676 heart-hand syndrome type 3 RGO:28676 RGO:28679 Naguib-Richieri-Costa syndrome RGO:28679 ORDO:2934 RGO:28681 polysyndactyly and congenital heart disease RGO:28681 syndactyly type 2 DOID:0060242 SNOMEDCT:715724002 RGO:28686 synpolydactyly RGO:28686 ORDO:921 RGO:28688 Abruzzo-Erickson syndrome RGO:28688 Al-Awadi Raas-Rothschild limb-pelvis hypoplasia-aplasia Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome limb/pelvis-hypoplasia/aplasia syndrome phocomelia Schinzel type RGO:28689 Al Awadi/Raas-Rothschild syndrome RGO:28689 RGO:28690 autosomal dominant microcephaly and radioulnar synostosis RGO:28690 RGO:28691 Cenani-Lenz type syndactyly RGO:28691 48,XXXX syndrome quadruple X tetra X tetrasomy X SNOMEDCT:10567003 RGO:28692 XXXX syndrome RGO:28692 ORDO:96263 SNOMEDCT:78317008 RGO:28693 XXXY syndrome RGO:28693 RGO:28696 familial humeroradial synostosis RGO:28696 RGO:28697 familial radioulnar synostosis-craniosynostosis RGO:28697 RGO:28698 sporadic humeroradial synostosis RGO:28698 RGO:28700 humeroradial-multiple synostosis syndrome RGO:28700 ORDO:2633 RGO:28701 mesomelic dysplasia Nievergelt type RGO:28701 radio-ulnar synostosis with amegakaryocytic thrombocytopenia RGO:28705 radioulnar synostosis and thrombocytopenia RGO:28705 RGO:28706 Tsukahara syndrome RGO:28706 Pfeiffer-Kapferer syndrome deafness - genital anomalies - metacarpal and metatarsal synostosis RGO:28711 sensorineural deafness - hypospadias - synostosis of metacarpals RGO:28711 RGO:28713 congenital ball-socket anomaly RGO:28713 RGO:28715 FGFR-opathy Muenke type RGO:28715 DOID:0060379 RGO:28726 acrofacial dysostosis RGO:28726 RGO:28727 acrorenal-ocular syndrome RGO:28727 DOID:0110971 HP:0005627 RGO:28728 brachydactyly type D RGO:28728 RGO:28732 osteosarcoma-absent thumbs syndrome RGO:28732 RGO:28735 radial hypoplasia syndrome RGO:28735 RGO:28739 familial preaxial polydactyly and triphalangeal thumb RGO:28739 RGO:28740 familial triphalangeal thumb RGO:28740 RGO:28741 isolated triphalangeal thumb RGO:28741 RGO:28751 absent tibia-triphalangeal thumb-polydactyly RGO:28751 RGO:28753 Carraro syndrome RGO:28753 ORDO:1986 RGO:28755 Gollop-Wolfgang complex RGO:28755 RGO:28756 isolated congenital tibial deficiency RGO:28756 RGO:28758 tibial hemimelia diplodia syndrome RGO:28758 Werner mesomelic dysplasia adult progeria DOID:5688 ORDO:902 SNOMEDCT:51626007 RGO:28759 Werner syndrome RGO:28759 RGO:28763 Greig cephalopolydactyly syndrome RGO:28763 RGO:28764 cardiomelic syndrome with ulnar agenesis RGO:28764 RGO:28765 carpal coalition plus RGO:28765 ORDO:1625 RGO:28766 chromosome 4q deletion RGO:28766 RGO:28767 craniosynostosis-ulnar aplasia RGO:28767 RGO:28768 familial ulnar aplasia and lobster claw syndrome RGO:28768 RGO:28770 Klippel-Feil syndrome-absent ulna RGO:28770 Langer mesomelic dysplasia ORDO:2632 RGO:28771 mesomelic dysplasia Langer type RGO:28771 RGO:28774 autosomal dominant isolated congenital vertical talus RGO:28774 RGO:28775 familial congenital vertical talus RGO:28775 DOID:0080074 HP:0045005 RADLEX:RID34598 SNOMEDCT:253098009 RGO:28776 neural tube defect RGO:28776 RGO:28778 adenosine deaminase deficiency with severe combined immunodeficiency and chondroosseous dysplasia RGO:28778 Morquio syndrome type A galactosamine-6-sulfatase deficiency ORDO:309297 RGO:28779 mucopolysaccharidosis type 4A RGO:28779 RGO:28782 spondylometaphyseal dysplasia East African type RGO:28782 ORDO:66637 RGO:28785 diaphanospondylodysostosis RGO:28785 SNOMEDCT:423095007 RGO:28786 molded baby syndrome RGO:28786 RGO:28790 familial protrusio acetabuli RGO:28790 RGO:28791 idiopathic chondrolysis of the hip RGO:28791 RGO:28800 chromosome dup(9p) trisomy syndrome RGO:28800 RGO:28801 familial pubic bone maldevelopment RGO:28801 ischio-spinal dysostosis ischio-vertebral syndrome ORDO:85200 SNOMEDCT:715654001 RGO:28802 ischio-vertebral dysplasia RGO:28802 ORDO:239 SNOMEDCT:82699004 RGO:28804 Dyggve-Melchior-Clausen syndrome RGO:28804 HP:0000039 ICD10CM:Q64.0 ORDO:93928 SNOMEDCT:406476007 RGO:28806 epispadias RGO:28806 ectopia vesicae exstrophy of the bladder DOID:0080174 HP:0002836 ORDO:93930 RGO:28807 bladder exstrophy RGO:28807 RGO:28808 imperforate anus with rectovaginal fistula RGO:28808 RGO:28809 isolated symphyseal diastasis RGO:28809 SNOMEDCT:75564005 RGO:28810 osteitis pubis RGO:28810 RGO:28811 pubic hypoplasia RGO:28811 RGO:28814 urethral duplication RGO:28814 Saldino-Noonan syndrome short rib-polydactyly syndrome Saldino-Noonan type RGO:28815 short rib-polydactyly syndrome type 1 RGO:28815 RADLEX:RID3464 SNOMEDCT:89902003 RGO:28816 Grisel syndrome RGO:28816 RGO:28817 incompetent transverse atlantoaxial ligament RGO:28817 RGO:28818 nontraumatic atlantoaxial subluxation RGO:28818 RGO:28819 odontoid anomaly RGO:28819 RGO:28820 Retropharyngeal or nasopharyngeal inflammation RGO:28820 RGO:28822 idiopathic intervertebral disk calcification RGO:28822 RGO:28823 deferoxamine treatment RGO:28823 ORDO:1787 RGO:28824 acrofacial dysostosis Palagonia type RGO:28824 RGO:28825 craniovertebral junction anomaly RGO:28825 RGO:28828 dappled dysplasia RGO:28828 RGO:28832 lethal skeletal dysplasia-CNS degeneration RGO:28832 DOID:12559 ORDO:85193 RGO:28835 idiopathic juvenile osteoporosis RGO:28835 DOID:10241 ICD10CM:D56 RADLEX:RID34418 SNOMEDCT:40108008 RGO:28837 thalassemia RGO:28837 RGO:28840 ectopic prostate tissue RGO:28840 RGO:28841 familial presacral mass RGO:28841 RADLEX:RID3922 SNOMEDCT:253127008 RGO:28842 neuroenteric cyst RGO:28842 RGO:28844 familial lumbar canal stenosis RGO:28844 atypical Scheuermann disease RGO:28846 juvenile lumbar osteochondrosis RGO:28846 RGO:28847 osteopathia striata-like syndrome RGO:28847 RGO:28849 3-M-like syndrome RGO:28849 RGO:28850 intraspinal neoplasm RGO:28850 mucosa-lined hemiperineal anomaly RGO:28855 pseudo-tail RGO:28855 RGO:28856 tail-tethered cord association RGO:28856 HP:0030725 ORDO:268865 RADLEX:RID3922 SNOMEDCT:41353005 RGO:28865 neurenteric cyst RGO:28865 DOID:4258 ORDO:3450 SNOMEDCT:699313003 RGO:28875 Weissenbacher-Zweymüller syndrome RGO:28875 RGO:28876 Berk-Tabatznik syndrome RGO:28876 BRESHECK syndrome ORDO:85284 RGO:28877 BRESEK syndrome RGO:28877 ORDO:1756 RGO:28878 caudal duplication RGO:28878 RGO:28879 cerebrofaciothoracic dysplasia RGO:28879 RGO:28880 familial C1 posterior arch defect RGO:28880 ORDO:1926 SNOMEDCT:716020005 RGO:28881 diabetic embryopathy RGO:28881 RGO:28882 Dobrow syndrome RGO:28882 ORDO:2165 RGO:28884 holoprosencephaly with caudal dysgenesis RGO:28884 ICD10CM:Q00.2 ORDO:63259 SNOMEDCT:2438005 RGO:28885 iniencephaly RGO:28885 RGO:28886 lumbocostovertebral sequence RGO:28886 RGO:28887 Mathieu syndrome RGO:28887 vertebral anomaly-eye anomaly-cutis aplasia-short stature syndrome RGO:28891 VECS syndrome RGO:28891 RGO:28896 cleidocranial dysplasia-like syndrome RGO:28896 RGO:28898 hypoplastic clavicles and lateral scapular redirection RGO:28898 ORDO:2793 SNOMEDCT:441944007 RGO:28899 oto-onycho-peroneal syndrome RGO:28899 RGO:28901 scapuloilac dysostosis RGO:28901 RGO:28902 short clavicle syndrome RGO:28902 HP:0100656 RGO:28903 thoracoabdominal schisis RGO:28903 RGO:28905 clavicular overgrowth and cystic hygroma RGO:28905 RGO:28906 stress-induced osteolysis RGO:28906 HP:0006633 RGO:28907 glenoid hypoplasia RGO:28907 RGO:28908 Currarino-Silverman syndrome RGO:28908 RGO:28909 marfanoid craniosynostosis syndrome RGO:28909 DOID:0050451 ORDO:130 SNOMEDCT:418818005 RGO:28912 Brugada syndrome RGO:28912 RGO:28913 familial congenital pectus excavatum RGO:28913 MMR syndrome Neuhäuser megalocornea - mental retardation syndrome Neuhäuser syndrome megalocornea - intellectual deficit syndrome RGO:28914 MMMM syndrome RGO:28914 RGO:28916 sunken chest syndrome RGO:28916 HP:0000892 SNOMEDCT:66102006 RGO:28917 bifid ribs RGO:28917 RGO:28918 costoiliac impingement syndrome RGO:28918 RGO:28919 familial cervical rib RGO:28919 RGO:28920 intrathoracic rib RGO:28920 RGO:28922 pelvic digit RGO:28922 DOID:0110341 ORDO:216804 RGO:28925 osteogenesis imperfecta type 2 RGO:28925 RGO:28928 chromosome 1 partial deletion syndrome RGO:28928 RGO:28929 adenosine deaminase deficiency with severe combined immunodeficiency and chondrodysplasia RGO:28929 RGO:28930 spondylochondrodysplasia RGO:28930 SNOMEDCT:205649008 RGO:28931 trisomy 8 RGO:28931 RGO:28934 thoracic venous obstruction RGO:28934 RGO:28935 Kaufman-McKusick-like syndrome RGO:28935 RGO:28936 metaphyseal dysplasia Shwachman type RGO:28936 SNOMEDCT:205294008 RGO:28937 floppy infant RGO:28937 RGO:28940 congenital aggressive lipomatosis RGO:28940 ECMO SNOMEDCT:233573008 RGO:28941 extracorporeal membrane oxygenation RGO:28941 DOID:0080047 SNOMEDCT:22567005 RGO:28942 pseudoachondroplastic dysplasia RGO:28942 RGO:28943 thickened cortical bones and congenital neutropenia RGO:28943 RGO:28944 vibrator chest physiotherapy in neonates RGO:28944 RGO:28945 geoderma osteodysplastica hereditaria RGO:28945 RGO:28946 sickle-shaped scapula RGO:28946 RGO:28947 snapping scapula syndrome RGO:28947 RGO:28948 Sprengel shoulder deformity RGO:28948 RGO:28949 thanatophoric variant Luton type RGO:28949 DOID:11476 HP:0000939 RADLEX:RID5389 SNOMEDCT:64859006 RGO:28951 osteoporosis RGO:28951 ORDO:3195 RGO:28954 sternal malformation-angiodysplasia association RGO:28954 RGO:28956 pterygium syndrome RGO:28956 RGO:28962 beekeeper arthropathy RGO:28962 DOID:10326 RGO:28963 Caplan syndrome RGO:28963 RGO:28964 Y chromosome deletion RGO:28964 RGO:28967 intestinal bypass syndrome RGO:28967 ICD10CM:M08.1 SNOMEDCT:239805001 RGO:28968 juvenile ankylosing spondylitis RGO:28968 NAO syndrome nodulosis-arthropathy-osteolysis syndrome RGO:28970 Al-Aqeel Sewairi syndrome RGO:28970 RGO:28971 osteolysis without nephropathy RGO:28971 RGO:28974 parvovirus arthropathy RGO:28974 RGO:28975 plant thorn-induced syndrome RGO:28975 chondrodysplasia punctata Happle type ORDO:35173 RGO:28976 chondrodysplasia punctata X-linked dominant type RGO:28976 SEMD-JL ORDO:93359 SNOMEDCT:254100000 RGO:28978 spondyloepimetaphyseal dysplasia with joint laxity RGO:28978 DOID:0050473 ORDO:64 SNOMEDCT:63702009 RGO:28980 Alström syndrome RGO:28980 RGO:28982 idiopathic familial advanced bone age RGO:28982 RGO:28983 lethal sclerotic skeletal dysplasia RGO:28983 RGO:28985 otospondylometaphyseal dysplasia RGO:28985 DOID:1206 ORDO:778 RADLEX:RID5166 SNOMEDCT:68618008 RGO:28986 Rett syndrome RGO:28986 SNOMEDCT:123527003 RGO:28987 sexual precocity RGO:28987 cerebral gigantism DOID:14748 ICD10CM:Q87.3 ORDO:821 SNOMEDCT:75968004 RGO:28988 Sotos syndrome RGO:28988 RGO:28999 deaf mutism-goiter-euthyroidism syndrome RGO:28999 DOID:0060439 ORDO:470 SNOMEDCT:303852004 RGO:29001 lysinuric protein intolerance RGO:29001 RGO:29002 Oliver-McFarlane syndrome RGO:29002 RGO:29004 Say syndrome RGO:29004 RGO:29008 idiopathic hip calcification in infants and children RGO:29008 MEN 2A multiple endocrine neoplasia 2A ORDO:247698 ORDO:653 RGO:29009 multiple endocrine neoplasia syndrome type 2A RGO:29009 RGO:29012 enchondromatosis-dwarfism-deafness RGO:29012 SNOMEDCT:389264005 RGO:29013 genochondromatosis RGO:29013 RGO:29017 tenosynovial chondromatosis RGO:29017 SNOMEDCT:239806000 RGO:29020 juvenile spondyloarthropathy RGO:29020 RGO:29022 retinoid therapy RGO:29022 calvarial doughnut lesions - bone fragility syndrome RGO:29027 calvarial doughnut lesions-osteoporosis-dentinogenesis imperfecta RGO:29027 RGO:29028 familial calvarial hyperostosis RGO:29028 RGO:29033 heel spur syndrome RGO:29033 Menkes kinky-hair syndrome Menkes syndrome kinky-hair syndrome DOID:1838 ORDO:565 SNOMEDCT:59178007 RGO:29039 Menkes disease RGO:29039 ORDO:52022 SNOMEDCT:702346005 RGO:29041 Potocki-Shaffer syndrome RGO:29041 DOID:13482 ORDO:744 SNOMEDCT:23150001 RGO:29042 Proteus syndrome RGO:29042 RGO:29043 radiation-induced osteochondroma RGO:29043 SNOMEDCT:4106009 RGO:29044 rotator cuff tear RGO:29044 DOID:13724 ICD10CM:E54 RADLEX:RID34649 SNOMEDCT:76169001 RGO:29045 scurvy RGO:29045 SCID severe combined immunodeficiency RGO:29046 severe combined immune deficiency RGO:29046 Majewski polydactyly syndrome Majewski syndrome short rib-polydactyly syndrome Majewski type short-rib polydactyly syndrome type 2 RGO:29047 short rib-polydactyly syndrome type 2 RGO:29047 RGO:29049 supracondylar humeral process RGO:29049 ORDO:93299 RGO:29053 achondrogenesis type 1A RGO:29053 diaphyseal medullary stenosis with bone malignancy RGO:29054 diaphyseal medullary stenosis with bone malignancy Hardcastle type RGO:29054 GM1 gangliosidosis several forms Landing disease Norman-Landing disease ICD10CM:E75.19 ORDO:354 SNOMEDCT:238025006 RGO:29055 GM1 gangliosidosis RGO:29055 Raine dysplasia RGO:29056 lethal osteosclerotic skeletal dysplasia Raine type RGO:29056 RGO:29057 Lichtenstein syndrome RGO:29057 RGO:29061 Werdnig-Hoffmann syndrome RGO:29061 ORDO:79233 RGO:29062 Kelley-Seegmiller syndrome RGO:29062 ICD10CM:E88.81 SNOMEDCT:237602007 RGO:29063 metabolic syndrome RGO:29063 RGO:29064 molybdenum excess RGO:29064 RGO:29065 reflex sympathetic dystrophy syndrome RGO:29065 RGO:29069 macrocephaly-cutis marmorata telangiectasia congenita RGO:29069 ORDO:1190 SNOMEDCT:43814000 RGO:29076 atelosteogenesis type 1 RGO:29076 RGO:29077 baby-rattle dysplasia RGO:29077 RGO:29080 harlequin fetus and micromelia RGO:29080 RGO:29084 metatropic dysplasia lethal type RGO:29084 RGO:29087 short rib syndrome Beemer type RGO:29087 RGO:29093 spondylometaphyseal abnormalities-advanced bone age RGO:29093 RGO:29094 spondylometaphyseal dysplasia Sedaghation type RGO:29094 RADLEX:RID3594 RGO:29096 calcium hydroxyapatite crystal deposition disease RGO:29096 RADLEX:RID3967 RGO:29097 cystic angiomatosis RGO:29097 RGO:29102 microgeodic disease RGO:29102 NS/MGCLS RGO:29104 Noonan-like/multiple giant-cell lesion syndrome RGO:29104 RGO:29106 phalangeal microgeodic syndrome of infancy RGO:29106 RGO:29110 osteolysis of the distal clavicle RGO:29110 RGO:29112 ear-ossicle osteolysis RGO:29112 RGO:29113 hyaline fibromatosis RGO:29113 RGO:29114 multicentric osteolysis RGO:29114 RGO:29116 Côté-Katasantoni syndrome RGO:29116 RGO:29118 familial infantile osteopetrosis and Hirschsprung disease RGO:29118 SNOMEDCT:707145005 RGO:29119 florid reactive periostitis RGO:29119 RGO:29120 hepatitis C-associated osteosclerosis RGO:29120 RGO:29127 myelofibrosis-osteosclerosis syndrome RGO:29127 RGO:29128 Nakamura disease RGO:29128 RGO:29130 physiologic osteosclerosis of newborns RGO:29130 SNOMEDCT:449777000 RGO:29133 transient infantile osteopetrosis RGO:29133 RGO:29134 trichorrhexis nodosa syndrome RGO:29134 chondrodysplasia punctata Conradi-Huenermann type RGO:29137 chondrodysplasia punctata Conradi-Hünermann type RGO:29137 RGO:29139 chondrodysplasia punctata Sheffield type RGO:29139 ORDO:79346 RGO:29140 chondrodysplasia punctata tibial-metacarpal type RGO:29140 RGO:29143 chromosome B:D translocation RGO:29143 RGO:29144 chromosome 7:16 translocation syndrome RGO:29144 Down syndrome ORDO:870 RGO:29146 trisomy 21 RGO:29146 RGO:29148 chromosome X;Y translocation RGO:29148 RGO:29149 fetal phenacetin exposure RGO:29149 RGO:29155 vitamin K epoxide reductase deficiency RGO:29155 RGO:29157 anticancer drug nephrotoxicity RGO:29157 RGO:29158 chronic ethane-1-hydroxy-1,1-diphosphonate intoxication RGO:29158 RGO:29159 epidermoid nevus syndrome RGO:29159 RGO:29160 ifosfamide nephrotoxicity RGO:29160 DOID:0050474 ORDO:634 SNOMEDCT:312514006 RGO:29162 Netherton syndrome RGO:29162 RGO:29163 oncogenic rickets RGO:29163 RGO:29165 Wilson syndrome RGO:29165 ORDO:113 SNOMEDCT:254820002 RGO:29170 Bazex-Dupre-Christol syndrome RGO:29170 RGO:29173 cutaneous McCune-Albright syndrome RGO:29173 ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome ORDO:1897 RGO:29174 EEM syndrome RGO:29174 GLH syndrome GLHS cerebello-trigeminal-dermal dysplasia cerebellotrigeminal dermal dysplasia ORDO:1532 RGO:29175 Gomez-López-Hernández syndrome RGO:29175 4-alpha-hydroxyphenylpyruvate hydroxylase deficiency ORDO:2118 SNOMEDCT:414380008 RGO:29176 hawkinsinuria RGO:29176 ORDO:90368 RGO:29177 hereditary hypotrichosis of the scalp RGO:29177 ORDO:330029 RGO:29178 hypotrichosis-deafness syndrome RGO:29178 ORDO:69735 RGO:29179 hypotrichosis-lymphedema-telangiectasia syndrome RGO:29179 ORDO:140936 RGO:29181 Lelis syndrome RGO:29181 RGO:29183 nail pitting and alopecia RGO:29183 seborrhea-acne-hirsutism-alopecia syndrome RGO:29185 SAHA syndrome RGO:29185 SNOMEDCT:2625009 RGO:29187 Senter syndrome RGO:29187 RGO:29188 Shokeir syndrome RGO:29188 ORDO:199282 SNOMEDCT:1407000100000410 RGO:29189 harlequin syndrome RGO:29189 RGO:29191 acro-cranio-facial dysostosis type 2 RGO:29191 RGO:29192 MSH6 mutation RGO:29192 RGO:29194 cutis tricolor RGO:29194 RGO:29195 familial café-au-lait spots RGO:29195 alopecia - anosmia - deafness - hypogonadism neuroectodermal syndrome Johnson type ORDO:2316 RGO:29196 Johnson-McMillin syndrome RGO:29196 ORDO:96175 RGO:29198 ring chromosome 11 RGO:29198 ORDO:3444 SNOMEDCT:403820003 SNOMEDCT:7425008 RGO:29199 Watson syndrome RGO:29199 familial arterial tortuosity DOID:0050645 ICD10CM:Q87.82 ORDO:3342 SNOMEDCT:458432002 RGO:29200 arterial tortuosity syndrome RGO:29200 RGO:29206 Bowen-Armstrong syndrome RGO:29206 AEC syndrome DOID:0090119 SNOMEDCT:55821006 RGO:29212 Hay-Wells syndrome RGO:29212 RGO:29214 uncombable hair syndrome plus RGO:29214 RGO:29215 chromosome 18 del(18q) syndrome RGO:29215 RGO:29218 spondyloepimetaphyseal dysplasia eczema/hypogammaglobinemia type RGO:29218 RGO:29219 Amish brittle hair syndrome RGO:29219 brittle hair-impaired intelligence-decreased fertility-short stature syndrome DOID:0050528 ORDO:1245 SNOMEDCT:403796005 RGO:29220 BIDS syndrome RGO:29220 Tay syndrome ichthyosis - brittle hair - impaired intelligence - decreased fertility - short stature syndrome trichothiodystrophy-plus DOID:2960 ORDO:453 RGO:29222 IBIDS syndrome RGO:29222 RGO:29223 methionine deficiency RGO:29223 DOID:2960 ORDO:33364 RGO:29226 trichothiodystrophy RGO:29226 RGO:29228 Elejalde syndrome 2 RGO:29228 PIBIDS photosensitivity - ichtyosis - brittle hair - intellectual deficit - decreased fertility - short statute trichothiodystrophy - sun sensitivity trichothiodystrophy type F ORDO:670 RGO:29238 PIBIDS syndrome RGO:29238 DOID:3263 HP:0007544 ICD10CM:E70.39 ORDO:2884 SNOMEDCT:718122005 RGO:29239 piebaldism RGO:29239 hepatolenticular degeneration DOID:893 ORDO:905 SNOMEDCT:88518009 RGO:29243 Wilson disease RGO:29243 SIOD Schimke immuno-osseous dysplasia RGO:29246 immuno-osseous dysplasia Schimke type RGO:29246 RGO:29247 primary palmar, plantar, and axillary hyperhidrosis RGO:29247 RGO:29248 speckled lentiginous nevus syndrome RGO:29248 Meleda disease Mljet disease ORDO:87503 RGO:29251 mal de Meleda RGO:29251 RGO:29252 Olmsted syndrome RGO:29252 RGO:29253 palmoplantar hyperkeratosis and sensorineural deafness RGO:29253 DOID:0111060 ORDO:1023 RGO:29256 Ambras syndrome RGO:29256 ORDO:528 RGO:29257 Berardinelli syndrome RGO:29257 RGO:29258 chromosome 14q deletion syndrome RGO:29258 DOID:0060471 RGO:29264 fetal valproic acid syndrome RGO:29264 hairy elbow syndrome HP:0004780 RGO:29265 hypertrichosis cubiti RGO:29265 SNOMEDCT:201159000 RGO:29268 idiopathic hypertrichosis RGO:29268 SNOMEDCT:111307005 RGO:29269 Leprechaunism syndrome RGO:29269 DOID:0060488 ORDO:2896 SNOMEDCT:702344008 RGO:29273 Pitt-Hopkins syndrome RGO:29273 DOID:13268 SNOMEDCT:418470004 RGO:29274 porphyria RGO:29274 HP:0012329 ORDO:1063 SNOMEDCT:705155008 RGO:29275 tufted angioma RGO:29275 Macias Flores-Garcia Cruz-Rivera syndrome X-linked congenital generalized hypertrichosis congenital generalized hypertrichosis Macias-Flores type ORDO:79495 RGO:29277 X-linked hypertrichosis RGO:29277 Chanarin-Dorfman syndrome ORDO:98907 RGO:29281 Dorfman-Chanarin syndrome RGO:29281 DOID:0060713 ORDO:457 SNOMEDCT:205548006 RGO:29282 Harlequin ichthyosis RGO:29282 Stormorken-Sjaastad-Langslet syndrome thrombocytopathy - asplenia - miosis DOID:0060354 ORDO:3204 SNOMEDCT:711407000 RGO:29287 Stormorken syndrome RGO:29287 HP:0001057 ICD10CM:Q84.8 SNOMEDCT:35484002 RGO:29292 aplasia cutis congenita RGO:29292 brachymesodactyly type A4 RGO:29295 brachymesophalangy-nail dysplasia RGO:29295 RGO:29298 double fingernails on fifth fingers RGO:29298 COIF COIF syndrome congenital onychodysplasia congenital onychodysplasia of the index fingers SNOMEDCT:403281007 RGO:29303 Iso-Kikuchi syndrome RGO:29303 ORDO:79143 RGO:29304 familial anonychia RGO:29304 RGO:29305 laryngoonychocutaneous syndrome RGO:29305 RGO:29309 trichoodontoonychial dysplasia RGO:29309 RGO:29310 triphalangeal thumb-onychodystrophy-deafness syndrome RGO:29310 RGO:29311 twenty-nail dystrophy and IgA deficiency RGO:29311 DOID:0050658 SNOMEDCT:1271009 RGO:29314 Bart-Pumphrey syndrome RGO:29314 SNOMEDCT:95320005 RGO:29315 dermatosis RGO:29315 RGO:29316 green nail syndrome RGO:29316 ORDO:2387 RGO:29317 leukonychia totalis RGO:29317 RGO:29318 shell nail syndrome RGO:29318 RGO:29319 congenital onycholysis RGO:29319 SNOMEDCT:403301006 RGO:29320 drug-induced onycholysis RGO:29320 RGO:29321 housewife onycholysis RGO:29321 HP:0008404 SNOMEDCT:87065009 RGO:29322 onychodystrophy RGO:29322 DOID:0050275 HP:0012203 ICD10CM:B35.1 SNOMEDCT:414941008 RGO:29323 onychomycosis RGO:29323 RGO:29324 acquired C1 inhibitor deficiency RGO:29324 SNOMEDCT:397768002 RGO:29325 cold panniculitis RGO:29325 RGO:29326 fasciitis-panniculitis syndrome RGO:29326 RGO:29327 halogen panniculitis RGO:29327 Winkelmann cytophagic panniculitis cytophagic histiocytic panniculitis ORDO:94087 RGO:29329 histiocytic cytophagic panniculitis RGO:29329 RGO:29330 infectiois panniculitis RGO:29330 RGO:29331 lupus profundus RGO:29331 ICD10CM:K65.4 RGO:29333 mesenteric panniculitis RGO:29333 SNOMEDCT:21586000 RGO:29334 Munchausen syndrome RGO:29334 RGO:29335 neutrophilic panniculitis RGO:29335 RGO:29336 steroid medication RGO:29336 RGO:29337 Rothman-Makai type panniculitis RGO:29337 ICD10CM:P83.0 SNOMEDCT:206539008 RGO:29338 sclerema neonatorum RGO:29338 RGO:29339 subcutaneous fat necrosis RGO:29339 RGO:29340 subcutaneous polyarteritis nodosa RGO:29340 RGO:29344 Ehlers-Danlos RGO:29344 localized fibrosing scleroderma localized scleroderma ORDO:90289 RGO:29346 focal scleroderma RGO:29346 Weary-Kindler syndrome acrokeratotic poikiloderma bullous acrokeratotic poikiloderma of Kindler and Weary congenital poikiloderma with blisters and keratoses congenital poikiloderma with bullae and progressive cutaneous atrophy hereditary acrokeratotic poikiloderma hereditary acrokeratotic poikiloderma of Kindler-Weary hyperkeratosis-hyperpigmentation syndrome DOID:0060472 ORDO:2908 ORDO:306539 SNOMEDCT:238836000 RGO:29347 Kindler syndrome RGO:29347 ORDO:1571 SNOMEDCT:703542000 RGO:29348 Knobloch syndrome RGO:29348 RGO:29349 occipital scalp defect and valvular pulmonary stenosis RGO:29349 RGO:29350 oculoectodermal syndrome RGO:29350 SNOMEDCT:403771007 RGO:29351 Setleis syndrome RGO:29351 DOID:6543 ICD10CM:L70.0 SNOMEDCT:88616000 RGO:29353 acne vulgaris RGO:29353 calcinosis cutis-osteoma cutis-poikiloderma-skeletal abnormalities syndrome RGO:29355 COPS syndrome RGO:29355 RGO:29356 basal cell skin cancer RGO:29356 RGO:29358 multiple heel sticks RGO:29358 RADLEX:RID3382 SNOMEDCT:23583003 SNOMEDCT:257552002 RGO:29361 inflammation RGO:29361 SNOMEDCT:13136005 RGO:29362 injection site RGO:29362 RGO:29363 intravenous calcium salt administration RGO:29363 DOID:8472 HP:0012344 SNOMEDCT:201049004 RGO:29365 morphea RGO:29365 RGO:29366 osteoma cutis and hemihypertrophy RGO:29366 RGO:29368 primary osteoma cutis RGO:29368 RADLEX:RID3829 SNOMEDCT:12402003 SNOMEDCT:275322007 RGO:29369 scar RGO:29369 RGO:29370 solitary congenital nodular calcification RGO:29370 SNOMEDCT:239094006 RGO:29371 subcutaneous fat necrosis of newborn RGO:29371 Lyell syndrome ORDO:95455 SNOMEDCT:23067006 RGO:29372 toxic epidermal necrolysis RGO:29372 SNOMEDCT:77016009 RGO:29373 amyoplasia congenita disruptive sequence RGO:29373 SNOMEDCT:34536000 RGO:29374 amniocentesis RGO:29374 RGO:29375 chromosome 9p duplication RGO:29375 RGO:29376 chromosome 18q deletion RGO:29376 RGO:29378 congenital symmetric skin dimples RGO:29378 DOID:2722 SNOMEDCT:8197001 RGO:29380 acrodermatitis RGO:29380 DOID:14755 ORDO:23 SNOMEDCT:41013004 RGO:29381 argininosuccinic aciduria RGO:29381 DOID:0050810 ICD10CM:E53.8 SNOMEDCT:413652008 RGO:29382 biotin deficiency RGO:29382 RGO:29383 Gianotti-Crosti disease RGO:29383 DOID:0050854 ICD10CM:M04.2 ORDO:575 SNOMEDCT:15123008 RGO:29385 Muckle-Wells syndrome RGO:29385 SNOMEDCT:702449004 RGO:29386 Nakajo syndrome RGO:29386 RGO:29390 cutis marmorata and leg length discrepancy RGO:29390 DOID:14500 ICD10CM:E77.1 ORDO:349 SNOMEDCT:64716005 RGO:29392 fucosidosis RGO:29392 restrictive dermopathy ORDO:2833 RGO:29399 stiff skin syndrome RGO:29399 RGO:29400 reticular erythematous mucinosis syndrome RGO:29400 XP DOID:0050427 ICD10CM:Q82.1 ORDO:910 SNOMEDCT:44600005 RGO:29401 xeroderma pigmentosum RGO:29401 acro-dermato-ungual-lacrimal-tooth syndrome DOID:0050601 ORDO:978 RGO:29403 ADULT syndrome RGO:29403 RGO:29405 carbon baby RGO:29405 RGO:29407 chromosomal mosaicism RGO:29407 RGO:29409 Goeminne syndrome RGO:29409 RGO:29411 infantile digital fibromatosis-pigmentary defects syndrome RGO:29411 lentigines-atrial myxoma-mucocutaneous myxoma-blue nevi syndrome DOID:0050471 RGO:29412 LAMB syndrome RGO:29412 RGO:29413 congenital pigmented nevus and rhabdomyosarcoma RGO:29413 RGO:29414 tyrosinase-deficient oculocutaneous albinism RGO:29414 Bonnet-Dechaume-Blanc syndrome Brégeat syndrome oculocerebral angiomatosis retinomesencephalic angiomatosis ORDO:53719 SNOMEDCT:6729006 RGO:29415 Wyburn-Mason syndrome RGO:29415 RGO:29417 perifollicular fibromas and skin tags RGO:29417 DOID:0050660 ORDO:1555 SNOMEDCT:703528008 RGO:29418 Beare-Stevenson cutis gyrata syndrome RGO:29418 RGO:29420 isolated auricular skin tag anomaly RGO:29420 ORDO:1665 RGO:29421 fetal brain disruption sequence RGO:29421 MLS syndrome ORDO:2556 RGO:29426 microphthalmia - linear skin defects syndrome RGO:29426 RGO:29427 nevus sebaceus of Jadassohn RGO:29427 RT radiotherapy RADLEX:RID39262 RGO:29428 radiation therapy RGO:29428 RGO:29429 Preceding scar from burn or trauma RGO:29429 RGO:29430 Li-Fraumeni cancer family syndrome RGO:29430 hereditary chronic nephritis hereditary nephritis DOID:10983 ICD10CM:Q87.81 ORDO:63 RADLEX:RID5296 RGO:29431 Alport syndrome RGO:29431 RGO:29432 autosomal dominant familial angiolipomatosis RGO:29432 FAMMM syndrome RGO:29433 familial atypical multiple mole-melanoma syndrome RGO:29433 ORDO:145 RGO:29434 familial breast/ovarian cancer RGO:29434 RGO:29435 familial cardiac myxoma RGO:29435 RGO:29436 familial central nervous system tumor RGO:29436 RGO:29437 familial lentiginosis RGO:29437 RGO:29438 familial leukemia RGO:29438 ORDO:99361 RGO:29440 familial isolated medullary thyroid carcinoma RGO:29440 DOID:6846 ORDO:618 RGO:29441 familial melanoma RGO:29441 RGO:29442 familial neural crest tumor RGO:29442 ORDO:1333 RGO:29443 familial pancreatic cancer RGO:29443 RGO:29444 familial renal neoplasm RGO:29444 DOID:4648 ORDO:357027 RGO:29445 familial retinoblastoma RGO:29445 RGO:29446 familial syndrome of cutaneous malignant melanoma and cerebral astrocytoma RGO:29446 RGO:29449 Lynch syndrome 1 RGO:29449 RGO:29450 Lynch syndrome 2 RGO:29450 RGO:29452 mirror-image lung adenocarcinoma in mirror-image twins RGO:29452 MEN 1 multiple endocrine neoplasia type 1 SNOMEDCT:30664006 RGO:29453 multiple endocrine neoplasia syndrome type 1 RGO:29453 pigmented dermatofibrosarcoma protuberans SNOMEDCT:398670003 SNOMEDCT:62621002 RGO:29455 Bednar tumor RGO:29455 SNOMEDCT:238865006 RGO:29456 fibromatosis colli RGO:29456 HP:0100882 SNOMEDCT:56364004 RGO:29457 fibrous hamartoma of infancy RGO:29457 RGO:29458 fibrous pleural tumor-hypoglycemia RGO:29458 DOID:0060466 HP:0000169 ICD10CM:K06.1 SNOMEDCT:58569000 RGO:29459 gingival fibromatosis RGO:29459 RGO:29460 infantile desmoid-type fibromatosis RGO:29460 HP:0025197 ORDO:199267 SNOMEDCT:399903008 RGO:29461 infantile digital fibromatosis RGO:29461 DOID:0080109 ORDO:2591 RADLEX:RID4299 SNOMEDCT:254146000 SNOMEDCT:73767002 RGO:29462 infantile myofibromatosis RGO:29462 SNOMEDCT:703633001 RGO:29463 lipofibromatosis RGO:29463 RGO:29464 malignant fibrous histiocytoma-opsoclonus-myoclonus syndrome RGO:29464 SNOMEDCT:274901004 SNOMEDCT:44155009 RGO:29465 calcifying epithelioma of Malherbe RGO:29465 cutaneomeningospinal angiomatosis ORDO:53721 SNOMEDCT:254774003 RGO:29466 Cobb syndrome RGO:29466 RGO:29469 familial nevus flammeus RGO:29469 RGO:29470 Gorham syndrome RGO:29470 RGO:29472 macrocephaly-cutis marmorata-telangiectasia congenita RGO:29472 Crow-Fukase syndrome PEP syndrome POEMS disease POEMS myeloma Takatsuki disease Takatsuki syndrome osteosclerotic myeloma polyneuropathy - endocrinopathy - plasma cell dyscrasia DOID:14039 ORDO:2905 SNOMEDCT:79268002 RGO:29473 POEMS syndrome RGO:29473 RGO:29474 ovarian hemangioma RGO:29474 ORDO:59315 SNOMEDCT:442300000 RGO:29475 rhombencephalosynapsis RGO:29475 RGO:29476 sacral hemangiomas and multiple congenital anomalies RGO:29476 RGO:29478 Vascular syndromes RGO:29478 DOID:4967 HP:0008221 SNOMEDCT:419920004 RGO:29481 adrenal hyperplasia RGO:29481 HP:0000840 SNOMEDCT:267395000 RGO:29482 adrenogenital syndrome RGO:29482 HP:0001022 ICD10CM:E70.3 SNOMEDCT:15890002 RGO:29483 albinism RGO:29483 ORDO:166113 SNOMEDCT:254820002 RGO:29486 Bazex syndrome RGO:29486 RGO:29488 Clark-Howel-Evans-McConnell syndrome RGO:29488 DOID:0050469 ORDO:3071 SNOMEDCT:309776008 RGO:29489 Costello syndrome RGO:29489 RGO:29490 Doege-Potter syndrome RGO:29490 pancytopenia-dysmelia syndrome DOID:13636 ORDO:84 SNOMEDCT:30575002 RGO:29495 Fanconi anemia RGO:29495 ORDO:144 SNOMEDCT:315058005 RGO:29499 hereditary nonpolyposis colon cancer RGO:29499 ORDO:99880 SNOMEDCT:702378002 RGO:29500 hyperparathyroidism-jaw tumor syndrome RGO:29500 HP:0004923 ORDO:238583 SNOMEDCT:68528007 RGO:29501 hyperphenylalaninemia RGO:29501 DOID:0050214 ORDO:43393 RGO:29503 Lambert-Eaton syndrome RGO:29503 enchondromatosis with hemangiomata DOID:0060221 ORDO:163634 RADLEX:RID4131 SNOMEDCT:46041001 RGO:29505 Maffucci syndrome RGO:29505 SNOMEDCT:56989000 RGO:29508 myasthenic syndrome RGO:29508 RGO:29509 nephrogenic hepatic dysfunction syndrome RGO:29509 RGO:29512 oral leukoplakia associated with tylosis and esophageal carcinoma RGO:29512 ORDO:2760 RGO:29513 OSLAM syndrome RGO:29513 RGO:29517 pleuropulmonary blastoma-Wilms tumor association RGO:29517 DOID:3132 ICD10CM:E80.1 ORDO:101330 SNOMEDCT:61860000 RGO:29519 porphyria cutanea tarda RGO:29519 DOID:1703 ICD10CM:C91.1 SNOMEDCT:277550009 RGO:29520 Richter syndrome RGO:29520 RGO:29523 thymic tumor syndrome RGO:29523 migrating thrombophlebitis thrombophlebitis migrans RGO:29524 Trousseau syndrome RGO:29524 ICD10CM:E88.3 SNOMEDCT:277605001 RGO:29525 tumor lysis syndrome RGO:29525 XO syndrome monosomy X syndrome DOID:3491 ORDO:881 RADLEX:RID34720 SNOMEDCT:38804009 RGO:29526 Turner syndrome RGO:29526 DOID:14515 ORDO:893 SNOMEDCT:715215007 RGO:29527 WAGR syndrome RGO:29527 RGO:29529 Wilms tumor-multiple lung hamartomas RGO:29529 SNOMEDCT:77121009 RGO:29530 X-linked lymphoproliferative syndrome RGO:29530 RGO:29531 xeroderma pigmentosa syndrome RGO:29531 RGO:29533 asplenia with liver malformation RGO:29533 RGO:29536 chromosome 15q deletion RGO:29536 RGO:29537 congenital obstructive uropathy-renal hamartoma-nephroblastomatosis RGO:29537 HP:0000085 RADLEX:RID35282 SNOMEDCT:41729002 RGO:29539 horseshoe kidney RGO:29539 DOID:3012 ORDO:524 SNOMEDCT:428850001 RGO:29542 Li-Fraumeni syndrome RGO:29542 RGO:29544 Wilms tumor-hyponatremic/hypertension syndrome RGO:29544 RGO:29546 antiretroviral therapy-induced lipoatrophy RGO:29546 ORDO:79344 RGO:29548 chondrodysplasia punctata dominant type RGO:29548 ORDO:1606 RGO:29553 chromosome 1p36 deletion RGO:29553 RGO:29556 familial hemihyperplasia RGO:29556 RGO:29557 idiopathic hemihypertrophy RGO:29557 ORDO:306669 RGO:29558 hemiparkinsonism-hemiatrophy syndrome RGO:29558 RGO:29560 hereditary hemihypertrophy-hemiparesis-hemiathetosis syndrome RGO:29560 RGO:29562 lymphatic vessel abnormality RGO:29562 acro-renal-ectodermal dysplasia-lipoatrophic-diabetes syndrome ORDO:1133 RGO:29576 AREDYLD syndrome RGO:29576 RGO:29577 familial unilateral giant breast RGO:29577 46,XX sex reversal 46,XX testicular disorder of sex development XX sex reversal de la Chapelle syndrome RGO:29578 XX male syndrome RGO:29578 SNOMEDCT:55644006 RGO:29579 thumb sucking RGO:29579 DOID:14181 ICD10CM:M65.2 SNOMEDCT:95414005 RGO:29583 calcific tendinitis RGO:29583 RGO:29584 calcium gluconate infiltration RGO:29584 RGO:29585 carbonate apatite deposition RGO:29585 RGO:29586 anterior longitudinal ligament ossification of the cervical spine in childhood RGO:29586 DOID:682 RADLEX:RID4953 SNOMEDCT:111245009 RGO:29587 compartment syndrome RGO:29587 RGO:29588 familial synovial chondromatosis and dwarfism RGO:29588 ORDO:2762 RGO:29594 progressive osseous heteroplasia RGO:29594 HP:0003201 ICD10CM:M62.82 RADLEX:RID5084 SNOMEDCT:240131006 SNOMEDCT:89010004 RGO:29595 rhabdomyolysis RGO:29595 RGO:29596 subcutaneous fat necrosis of the newborn and hypercalcemia RGO:29596 macrosomia-obesity-macrocephaly-ocular abnormality syndrome ORDO:2563 RGO:29609 MOMO syndrome RGO:29609 mental retardation, overgrowth, remarkable face and acanthosis nigricans RGO:29610 MORFAN RGO:29610 RGO:29612 trisomy 8 mosaicism RGO:29612 SNOMEDCT:205824006 RGO:29613 Turner-like syndrome RGO:29613 RGO:29616 central nervous system dysfunction in infancy RGO:29616 RGO:29617 sex chromosome disorder RGO:29617 RGO:29619 defective testosterone synthesis RGO:29619 RGO:29620 excessive extraglandular aromatase activity RGO:29620 RGO:29621 hereditary gynecomastia RGO:29621 SNOMEDCT:431498001 RGO:29622 idiopathic gynecomastia RGO:29622 DOID:1614 RGO:29623 male breast cancer RGO:29623 SNOMEDCT:48723006 RGO:29626 primary gonadal failure RGO:29626 RGO:29627 dialysis RGO:29627 SNOMEDCT:33927004 RGO:29628 secondary hypogonadism RGO:29628 RGO:29629 X-linked mental retardation - gynecomastia - obesity RGO:29629 ORDO:168632 RGO:29631 basaloid follicular hamartoma syndrome RGO:29631 ORDO:1297 RGO:29632 branchio-oculo-facial syndrome RGO:29632 RGO:29634 epiderma nevus syndrome RGO:29634 Von Meyemburg complexes RGO:29636 microhamartomatosis of the liver RGO:29636 RGO:29638 Wilms tumor and multiple lung hamartomas RGO:29638 RGO:29639 Weinberg-Zumwalt syndrome RGO:29639 alpha thalassemia DOID:1099 ORDO:846 RGO:29640 alpha-thalassemia RGO:29640 RGO:29641 Ballantyne syndrome RGO:29641 Di Guglielmo syndrome ICD10CM:C94.0 SNOMEDCT:14317002 SNOMEDCT:93451002 RGO:29642 erythroleukemia RGO:29642 SNOMEDCT:71028008 RGO:29643 fetomaternal transfusion RGO:29643 DOID:0110031 ICD10CM:D56.0 ORDO:93616 SNOMEDCT:48553001 RGO:29644 hemoglobin H disease RGO:29644 RGO:29645 hemorrhage into neoplasm RGO:29645 SNOMEDCT:14087004 RGO:29646 hereditary stomatocytosis RGO:29646 ORDO:667 RGO:29647 malignant osteopetrosis RGO:29647 RGO:29650 chromosome 11 partial duplication RGO:29650 RGO:29657 chromosome 22 long arm rearrangement RGO:29657 RGO:29660 agenesis of the ductus venosus RGO:29660 RGO:29667 fetal akinesia syndrome RGO:29667 RGO:29668 fetal hyperthyroidism RGO:29668 SNOMEDCT:82353009 RGO:29670 congenital infection RGO:29670 HP:0003568 ORDO:712 RGO:29671 glucosephosphate isomerase deficiency RGO:29671 idiopathic hydrops fetalis ORDO:89845 RGO:29674 idiopathic recurrent hydrops RGO:29674 RGO:29675 intrauterine dwarfism with thin bones and fractures RGO:29675 RGO:29676 isolated recurrent cystic hygroma RGO:29676 ORDO:2347 RGO:29677 lethal Kniest-like dysplasia RGO:29677 RGO:29680 maternal indomethacin therapy RGO:29680 HP:0030741 RGO:29681 mediastinal teratoma RGO:29681 I-cell disease Leroy syndrome mucolipidosis type II ORDO:576 RGO:29682 mucolipidosis type 2 RGO:29682 Morquio syndrome type B beta galactosidase deficiency ORDO:309310 RGO:29683 mucopolysaccharidosis type 4B RGO:29683 MPS 7 Sly syndrome beta-glucuronidase deficiency ORDO:584 RGO:29684 mucopolysaccharidosis type 7 RGO:29684 DOID:14504 ICD10CM:E75.242 ORDO:646 SNOMEDCT:66751000 RGO:29686 Niemann-Pick disease type C RGO:29686 RGO:29689 pulmonary neoplasm RGO:29689 sialic acid storage disease RGO:29693 sialic acid storage disorder RGO:29693 RGO:29694 thantophoric variant RGO:29694 DOID:8544 SNOMEDCT:52702003 RGO:29699 chronic fatigue syndrome RGO:29699 RGO:29701 familial enteropathy with villous edema and immunoglobulin G2 subclass deficiency RGO:29701 DOID:0060875 SNOMEDCT:234533006 RGO:29702 Fleisher syndrome RGO:29702 RGO:29709 phenylketonuria-related dysgammaglobulinemia RGO:29709 RGO:29711 small carpus RGO:29711 DOID:0060013 SNOMEDCT:203592006 RGO:29712 X-linked severe combined immunodeficiency RGO:29712 multiple hamartoma syndrome ORDO:201 SNOMEDCT:58037000 RGO:29713 Cowden syndrome RGO:29713 DOID:446 HP:0003118 ORDO:553 SNOMEDCT:237735008 RGO:29714 Cushing syndrome RGO:29714 RGO:29717 facial lipomatosis RGO:29717 ORDO:199279 RGO:29718 familial angiolipomatosis RGO:29718 RGO:29719 familial lipomatosis RGO:29719 RGO:29721 lipomatous melanocytic nevomatosis-plus RGO:29721 DOID:3926 RGO:29722 mediastinal lipomatosis RGO:29722 RGO:29724 chromosome 1 somatic translocation RGO:29724 RGO:29725 pericardial lipomatosis RGO:29725 ORDO:529 RGO:29727 Roch-Leri syndrome RGO:29727 RGO:29728 synovial lipomatosis RGO:29728 RGO:29729 chromosome 21q- disorder RGO:29729 SNOMEDCT:422437002 RGO:29730 Lujan-Fryns syndrome RGO:29730 ORDO:42775 RGO:29738 PHACE syndrome RGO:29738 myoclonic epilepsy and ragged red fibers DOID:310 ICD10CM:E88.42 ORDO:551 RGO:29740 MERRF syndrome RGO:29740 RGO:29743 dental sealant toxicity RGO:29743 RGO:29745 multiple angiomatosis RGO:29745 NCM Rokitansky-van Bogaert syndrome neurocutaneous melanocytosis ORDO:2481 RGO:29747 neurocutaneous melanosis RGO:29747 RGO:29749 oculodermal melanosis RGO:29749 RGO:29753 anterior thoracic hypoplasia RGO:29753 ORDO:2456 RGO:29754 familial supernumerary nipples RGO:29754 RGO:29755 autosomal dominant inverted nipples RGO:29755 RGO:29756 nipple vasospasm-Raynaud syndrome RGO:29756 Yunis-Varon dysplasia cleidocranial dysostosis with micrognathia and absent thumbs DOID:0060589 ORDO:3472 RGO:29760 Yunis-Varon syndrome RGO:29760 HP:0025027 SNOMEDCT:404074003 SNOMEDCT:71304002 RGO:29762 osteoma cutis RGO:29762 DOID:8616 RADLEX:RID3824 RGO:29763 Peyronie disease RGO:29763 ORDO:2875 SNOMEDCT:403545005 RGO:29771 phakomatosis pigmentovascularis RGO:29771 RGO:29772 glomangiomatosis of Bailey RGO:29772 RGO:29774 intestinal polyposis with multiple exostoses RGO:29774 HP:0200008 RGO:29775 intestinal polyposis RGO:29775 RGO:29776 juvenile polyposis with pulmonary arteriovenous malformation RGO:29776 RGO:29777 polyposis coli juvenile type RGO:29777 RGO:29778 familial polyposis of colon RGO:29778 RGO:29779 familial polyposis of entire alimentary tract RGO:29779 ORDO:211 RGO:29783 cylindromatosis RGO:29783 RGO:29784 Divry-Van Bogaert syndrome RGO:29784 SNOMEDCT:403825008 RGO:29786 epithelioma adenoides cysticum of Brooke RGO:29786 DOID:5981 HP:0002444 RGO:29788 hypothalamic hamartoma RGO:29788 RGO:29791 Porteus syndrome RGO:29791 SNOMEDCT:271020004 RGO:29796 amastia RGO:29796 RGO:29798 phalangeal hypoplasia with anonychia RGO:29798 RGO:29799 patches of lipodystrophy RGO:29799 RGO:29800 aplasia of the abdominal muscles RGO:29800 RGO:29802 hyperextensibility of joints RGO:29802 HP:0000490 RGO:29803 ocular depression RGO:29803 RGO:29806 lipodystrophy of the upper limbs RGO:29806 RGO:29807 lipodystrophy of the lower face RGO:29807 RGO:29808 diploid-triploid mosaicism RGO:29808 DOID:2494 RADLEX:RID3370 SNOMEDCT:71072006 SNOMEDCT:90858003 RGO:29809 angiodysplasia RGO:29809 RGO:29810 congenital varicose vein RGO:29810 RGO:29812 chronic spinal fluid lymphocytosis RGO:29812 RGO:29813 lenticulodentate calcification RGO:29813 HP:0002273 SNOMEDCT:91327001 RGO:29814 quadriparesis RGO:29814 DOID:0060230 HP:0002135 RGO:29815 basal ganglia calcification RGO:29815 RGO:29816 chondrocyte inclusion RGO:29816 RGO:29819 delayed development of speech RGO:29819 RGO:29823 nasal aplasia RGO:29823 RGO:29824 CNS anomaly RGO:29824 RGO:29825 absent cervical lymphoid tissue RGO:29825 RGO:29826 hypoplastic cervical lymphoid tissue RGO:29826 RGO:29827 inclusion tongue cysts RGO:29827 HP:0000465 SNOMEDCT:11731003 RGO:29828 webbed neck RGO:29828 DOID:0050328 HP:0000851 ORDO:442 SNOMEDCT:190268003 RGO:29831 congenital hypothyroidism RGO:29831 SNOMEDCT:276177000 RGO:29832 dysthyroid orbitopathy RGO:29832 RGO:29833 CNS abnormality RGO:29833 DOID:9840 HP:0000565 ICD10CM:H50.0 SNOMEDCT:16596007 RGO:29836 esotropia RGO:29836 DOID:10376 HP:0000646 SNOMEDCT:387742006 RGO:29837 amblyopia RGO:29837 ORDO:155878 SNOMEDCT:43437003 RGO:29838 submucous cleft palate RGO:29838 RGO:29840 hemimaxillary enlargement RGO:29840 RGO:29842 tooth anomaly RGO:29842 RGO:29843 skin findings RGO:29843 RGO:29844 hypertrichosis of the facial skin RGO:29844 RGO:29845 unilateral enlargement of the maxilla RGO:29845 RGO:29846 hypoplastic teeth RGO:29846 RGO:29847 unilateral parotid gland agenesis RGO:29847 HP:0011326 RGO:29848 frontal plagiocephaly RGO:29848 RGO:29849 familial hemifacial microsomia with radial limb defects RGO:29849 RGO:29850 otopalatodigital dysplasia RGO:29850 RGO:29851 nonerupting teeth-maxillozygomatic hypoplasia RGO:29851 RGO:29852 plantar lipomatosis RGO:29852 monobrow single eyebrow unibrow HP:0000664 SNOMEDCT:253207002 RGO:29853 synophrys RGO:29853 HP:0002223 RGO:29854 absent eyebrows RGO:29854 HP:0045075 RGO:29855 sparse eyebrows RGO:29855 HP:0002553 RGO:29856 arched eyebrows RGO:29856 HP:0000574 RGO:29857 heavy eyebrows RGO:29857 DOID:986 HP:0002229 ICD10CM:L63 SNOMEDCT:68225006 RGO:29861 alopecia areata RGO:29861 HP:0007418 ORDO:700 SNOMEDCT:19754005 RGO:29862 alopecia totalis RGO:29862 DOID:0050634 HP:0002289 ICD10CM:L63.1 ORDO:701 SNOMEDCT:86166000 RGO:29863 alopecia universalis RGO:29863 RGO:29864 medially flared eyebrows RGO:29864 RGO:29865 double eyebrows RGO:29865 split hand-split foot deformity split hand-split foot malformation ORDO:2440 RGO:29867 split hand and foot malformation RGO:29867 RGO:29868 genitourinary anomaly RGO:29868 RGO:29870 female siblings RGO:29870 RGO:29875 syndactyly of the feet RGO:29875 HP:0000308 RGO:29876 microretrognathia RGO:29876 RGO:29878 congenital defect of the anterior part of the maxillary bone RGO:29878 RGO:29879 absence of maxillary incisors and canines RGO:29879 HP:0009939 SNOMEDCT:91922000 RGO:29880 agnathia RGO:29880 HP:0100663 SNOMEDCT:77471004 RGO:29881 synotia RGO:29881 RGO:29883 hypognathia RGO:29883 SNOMEDCT:32958008 RGO:29884 congenital mandibular hypoplasia RGO:29884 HP:0000430 RGO:29885 hypoplastic nasal alae RGO:29885 RGO:29887 U-shaped cleft palate RGO:29887 DOID:13714 HP:0000674 ICD10CM:K00.0 ORDO:99797 SNOMEDCT:26624006 RGO:29888 anodontia RGO:29888 RGO:29889 vascular lesions with lymphoid and eosinophilic infiltrates RGO:29889 RGO:29890 cervical adenopathy RGO:29890 RGO:29892 periodic fever RGO:29892 RGO:29894 hemispheric paralysis of visual fixation RGO:29894 RGO:29895 optic ataxia RGO:29895 RGO:29896 visual attention disorder RGO:29896 SNOMEDCT:9345005 RGO:29897 dialysis dementia RGO:29897 RGO:29898 absence of tendon reflexes RGO:29898 RGO:29901 white matter disease RGO:29901 HP:0001251 SNOMEDCT:20262006 RGO:29902 ataxia RGO:29902 SNOMEDCT:251530001 RGO:29903 myoclonia RGO:29903 RGO:29904 visual failure RGO:29904 RGO:29905 ingestion of methylmercury-contaminated fish from Minamata Bay RGO:29905 HP:0002059 SNOMEDCT:278849000 RGO:29906 cerebral atrophy RGO:29906 HP:0001272 RGO:29907 cerebellar atrophy RGO:29907 RGO:29908 brainstem leukodystrophy RGO:29908 RGO:29909 subcortical white matter leukodystrophy RGO:29909 HP:0007256 RGO:29913 pyramidal signs RGO:29913 RGO:29914 hemosiderin deposition in the cranial nerves RGO:29914 RGO:29915 hemosiderin deposition in the leptomeninges RGO:29915 RGO:29916 hemosiderin deposition in the spinal cord RGO:29916 RGO:29917 infantile hypoglycemic hypoketotic encephalopathy RGO:29917 RGO:29918 Reye-like syndrome RGO:29918 RGO:29919 26-hydroxylase deficiency RGO:29919 RGO:29920 joint hypermobility and dislocations/subluxations RGO:29920 RGO:29921 skeletal abnormality RGO:29921 HP:0000271 RGO:29922 facial abnormality RGO:29922 HP:0000989 SNOMEDCT:418290006 RGO:29924 itching RGO:29924 RGO:29925 Sézary cells RGO:29925 SNOMEDCT:4830009 SNOMEDCT:49765009 RGO:29926 hyperpigmentation RGO:29926 RGO:29927 loss of hair and nails RGO:29927 RGO:29928 IgE hyperimmunoglobulinemia RGO:29928 HP:0001029 SNOMEDCT:402685001 SNOMEDCT:70114006 RGO:29930 poikiloderma RGO:29930 HP:0000992 SNOMEDCT:90128006 RGO:29932 photosensitivity RGO:29932 RGO:29934 urogenital anomaly RGO:29934 RGO:29938 VATER association and hydrocephalus RGO:29938 linear nevus sebaceous syndrome ORDO:2612 RGO:29941 linear nevus sebaceus syndrome RGO:29941 SNOMEDCT:88587007 RGO:29942 premature ageing RGO:29942 RGO:29943 cerebral falx calcification RGO:29943 RGO:29945 idiopathic nonarteriosclerotic intracerebral calcification RGO:29945 RGO:29946 retinal ischemic syndrome RGO:29946 RGO:29947 digestive-tract small vessel hyalinosis RGO:29947 RGO:29948 renal small vessel hyalinosis RGO:29948 RGO:29949 familial Coats reaction retinal angioma RGO:29949 RGO:29950 hair and nail defects RGO:29950 DOID:12377 HP:0007269 SNOMEDCT:5262007 RGO:29953 spinal muscular atrophy RGO:29953 SNOMEDCT:362969004 RGO:29954 endocrinopathy RGO:29954 RGO:29955 atrophic extraocular muscles RGO:29955 RGO:29956 extraocular muscle atrophy RGO:29956 RGO:29957 cardioskeletal myopathy RGO:29957 RGO:29958 laminopathy RGO:29958 HP:0003546 RGO:29959 exercise intolerance RGO:29959 RGO:29960 cramps RGO:29960 RGO:29961 myoglobulinuria RGO:29961 HP:0001927 RGO:29962 red cell acanthocytosis RGO:29962 RGO:29963 hypokalemic myopathy RGO:29963 HP:0000467 RGO:29964 neck muscle weakness RGO:29964 RADLEX:RID3323 SNOMEDCT:125236003 SNOMEDCT:277196008 RGO:29966 berry aneurysm RGO:29966 RGO:29967 bilateral symmetric cerebral calcifications RGO:29967 ORDO:226 SNOMEDCT:58256000 RGO:29968 dihydropteridine reductase deficiency RGO:29968 HP:0031291 RGO:29969 ichthyosis follicularis RGO:29969 SNOMEDCT:23323004 RGO:29970 atrichia RGO:29970 HP:0000613 ICD10CM:H53.14 SNOMEDCT:409668002 RGO:29971 photophobia RGO:29971 HP:0002715 RGO:29973 immunological abnormality RGO:29973 RGO:29974 agenesis corpus callosum RGO:29974 RGO:29975 clefting RGO:29975 HP:0008278 RGO:29976 cerebellar cortical atrophy RGO:29976 HP:0002514 SNOMEDCT:17944005 RGO:29977 cerebral calcification RGO:29977 RGO:29979 unilateral paralysis of all cranial nerves RGO:29979 HP:0000282 RGO:29981 facial edema RGO:29981 ORDO:2809 RGO:29982 relapsing peripheral facial palsy RGO:29982 RGO:29983 familial idiopathic acro-osteolysis RGO:29983 HP:0000164 RGO:29984 dental abnormality RGO:29984 RGO:29989 scapular/clavicular fibrous union RGO:29989 RGO:29990 defective ossification of skull RGO:29990 RGO:29991 defective ossification of clavicles RGO:29991 RGO:29992 mandibular clefting RGO:29992 HP:0008428 RGO:29993 vertebral clefting RGO:29993 HP:0003282 RGO:29994 low alkaline phosphatase RGO:29994 HP:0000270 RGO:29996 delayed fontanel closure RGO:29996 HP:0000894 RGO:29997 clavicular hypoplasia RGO:29997 SNOMEDCT:271807003 RGO:29998 skin eruption RGO:29998 RGO:29999 GU anomaly RGO:29999 RGO:30000 anterolateral displacement of the shoulders and scapulas on thoracic cage RGO:30000 RGO:30001 multiple ipsilateral osteoma cutis lesions RGO:30001 RGO:30002 contralateral hemihypertrophy RGO:30002 RGO:30003 hypodontia and/or early loss of permanent teeth RGO:30003 HP:0007385 RGO:30005 scalp defect RGO:30005 HP:0002561 RGO:30006 absent nipples RGO:30006 HP:0000598 RGO:30007 ear anomaly RGO:30007 DOID:11156 HP:0000970 ICD10CM:L74.4 SNOMEDCT:39659002 RGO:30008 anhidrosis RGO:30008 HP:0002164 RGO:30009 onychodysplasia RGO:30009 SNOMEDCT:4191007 RGO:30013 sagittal synostosis RGO:30013 HP:0009826 RGO:30015 short limbs RGO:30015 HP:0000144 SNOMEDCT:17276009 RGO:30017 decreased fertility RGO:30017 RGO:30020 moniliform hairs RGO:30020 ICD10CM:E50.8 SNOMEDCT:238625005 RGO:30021 follicular keratosis RGO:30021 HP:0001598 SNOMEDCT:66270006 RGO:30022 koilonychia RGO:30022 RGO:30024 abnormal crown morphology of the teeth RGO:30024 RGO:30026 degenerative brain disease RGO:30026 RGO:30027 polydactyly of hands and feet RGO:30027 HP:0002948 RADLEX:RID46050 RGO:30028 vertebral fusion RGO:30028 HP:0000164 RGO:30029 dental anomalies RGO:30029 HP:0011088 ICD10CM:K00.2 SNOMEDCT:55197001 RGO:30030 dens invaginatus RGO:30030 HP:0001572 ICD10CM:K00.2 SNOMEDCT:71485000 RGO:30031 macrodontia RGO:30031 HP:0001371 SNOMEDCT:385522000 RGO:30032 flexion contracture RGO:30032 RGO:30033 dense spine RGO:30033 RGO:30035 poor ossification of long bones RGO:30035 DOID:14227 HP:0000027 ICD10CM:N46.0 SNOMEDCT:425558002 SNOMEDCT:48188009 RGO:30036 azoospermia RGO:30036 RGO:30038 midline lipoma of central nervous system RGO:30038 HP:0000460 RGO:30039 thin nose RGO:30039 RGO:30041 ectopic adenoidal tissue in choanae RGO:30041 RGO:30042 combined valvular heart disease RGO:30042 RGO:30044 multiple left-to-right shunts RGO:30044 Ivemark syndrome absent spleen syndrome asplenia HP:0001746 SNOMEDCT:17604001 RGO:30045 asplenia syndrome RGO:30045 SNOMEDCT:72425000 RGO:30046 polysplenia syndrome RGO:30046 RGO:30047 anomalous systemic venous return to left atrium RGO:30047 HP:0000180 SNOMEDCT:253752000 RGO:30048 lobulated tongue RGO:30048 RGO:30049 tongue hamartoma RGO:30049 RGO:30050 orofaciodigital syndrome type 3 RGO:30050 oral-facial-digital syndrome type 4 RGO:30051 orofaciodigital syndrome type 4 RGO:30051 HP:0000519 RGO:30055 congenital cataracts RGO:30055 RGO:30058 missing lower central and lateral incisors RGO:30058 RGO:30059 supernumerary cuspids and bicuspids RGO:30059 RGO:30062 dysmorphism syndrome RGO:30062 RGO:30063 unusual nasal configuration RGO:30063 SNOMEDCT:254125009 RGO:30065 axial osteosclerosis RGO:30065 RGO:30067 dilated internal auditory meatus RGO:30067 ICD10CM:K04.2 SNOMEDCT:57602001 RGO:30068 denticles RGO:30068 HP:0000303 SNOMEDCT:22810007 RGO:30069 mandibular prognathism RGO:30069 RGO:30070 eye anomaly RGO:30070 RGO:30071 skin anomaly RGO:30071 HP:0007957 SNOMEDCT:64634000 RGO:30072 corneal opacity RGO:30072 ICD10CM:M62.83 RGO:30073 muscle spasm RGO:30073 HP:0000400 ICD10CM:Q17.1 SNOMEDCT:69056000 RGO:30074 macrotia RGO:30074 RADLEX:RID39179 SNOMEDCT:1372004 RGO:30076 uterus unicornis RGO:30076 RGO:30077 dermal aplasia RGO:30077 DOID:0060252 HP:0000647 RGO:30078 sclerocornea RGO:30078 DOID:10970 HP:0002510 SNOMEDCT:192965001 RGO:30079 spastic quadriplegia RGO:30079 RGO:30080 chromosome translocation syndrome RGO:30080 RGO:30081 chromosome duplication syndrome RGO:30081 RGO:30082 chromosome deletion syndrome RGO:30082 ORDO:96321 SNOMEDCT:72991005 RGO:30083 polyploidy syndrome RGO:30083 RGO:30084 chromosome polysomy syndrome RGO:30084 RGO:30085 trisomy syndrome RGO:30085 RGO:30091 forward trunk flexion RGO:30091 RGO:30092 phrenic nerve involvement RGO:30092 RGO:30093 bilateral hemidiaphragm paralysis/paradoxical motion RGO:30093 HP:0000902 RGO:30094 fused ribs RGO:30094 HP:0001609 RGO:30097 hoarse voice RGO:30097 RGO:30098 chronic skin ulceration RGO:30098 RGO:30101 dolichonychia RGO:30101 RGO:30102 nail dysgenesis RGO:30102 ICD10CM:Q77.2 SNOMEDCT:254050009 RGO:30105 short rib syndrome RGO:30105 HP:0001270 SNOMEDCT:307653008 RGO:30113 motor delay RGO:30113 RGO:30114 lipid storage disorder RGO:30114 RGO:30115 hair defect RGO:30115 RGO:30116 immune abnormality RGO:30116 DOID:4154 HP:0000703 ICD10CM:K00.5 ORDO:49042 SNOMEDCT:196286005 RGO:30122 dentinogenesis imperfecta RGO:30122 HP:0000098 SNOMEDCT:248328003 RGO:30123 tall stature RGO:30123 ICD10CM:E75.0 ORDO:309152 RGO:30124 GM2 gangliosidosis RGO:30124 ORDO:309246 RGO:30126 GM2 gangliosidosis AB variant RGO:30126 dermoid cyst RADLEX:RID3904 SNOMEDCT:417137001 RGO:30127 dermoid RGO:30127 HP:0100774 RGO:30128 bone overgrowth RGO:30128 HP:0004437 RGO:30129 cranial hyperostosis RGO:30129 RGO:30130 orofacial dyspraxia RGO:30130 HP:0000205 RGO:30133 pursed lips RGO:30133 HP:0001083 SNOMEDCT:74969002 RGO:30134 ectopia lentis RGO:30134 RGO:30135 chromosome 6q duplication RGO:30135 RGO:30136 chromosome 4p trisomy RGO:30136 RGO:30137 chromosome UPD 6 9DAS0 RGO:30137 RGO:30139 chromosome 12p trisomy RGO:30139 RGO:30140 tongue neoplasm RGO:30140 RGO:30141 cardiac defect RGO:30141 RGO:30143 ectrodactyly and syndactyly of the feet RGO:30143 RGO:30144 limb defects RGO:30144 RGO:30145 radial and fibular aplasia RGO:30145 RGO:30148 cutaneous polyps of the facial skin and nasal mucosa RGO:30148 RGO:30149 digital anomaly RGO:30149 HP:0002558 ICD10CM:Q83.3 SNOMEDCT:50956007 RGO:30153 supernumerary nipple RGO:30153 RGO:30154 superior nipple location RGO:30154 RGO:30155 nipple hypertrophy RGO:30155 RGO:30158 mucosal neuroma RGO:30158 HP:0025476 RGO:30159 testicular lipomatosis RGO:30159 RGO:30160 large subcutaneous angiolipomata RGO:30160 RGO:30161 painful subcutaneous lipoma RGO:30161 DOID:2487 HP:0003124 SNOMEDCT:13644009 RGO:30163 hypercholesterolemia RGO:30163 RGO:30164 pancreatic lipomatosis RGO:30164 RGO:30165 multiple familial circumscribed lipomatosis RGO:30165 RGO:30166 trisome 21 syndrome RGO:30166 RGO:30167 autosomal chromosome syndrome RGO:30167 RGO:30168 sex chromosome syndrome RGO:30168 RGO:30172 forked tip of tongue RGO:30172 DOID:11514 HP:0000221 ICD10CM:K14.5 SNOMEDCT:52368004 RGO:30173 furrowed tongue RGO:30173 RGO:30174 tongue ulcer RGO:30174 lingua cochlearis RGO:30175 spoon-shaped tongue RGO:30175 RGO:30177 tongue leukoplakia RGO:30177 HP:0030833 SNOMEDCT:81680005 RGO:30178 neck pain RGO:30178 RGO:30179 tongue paresthesia RGO:30179 RGO:30180 figure skating RGO:30180 RGO:30181 nontoxic thyroid enlargement RGO:30181 RGO:30182 clefting of the primary or secondary plate RGO:30182 RGO:30183 lower lip pits RGO:30183 RGO:30187 eye coloboma RGO:30187 RGO:30189 foot anomalies RGO:30189 HP:0012165 RGO:30190 oligodactyly RGO:30190 RGO:30191 hand anomaly RGO:30191 HP:0002058 RGO:30193 myopathic face RGO:30193 DOID:3650 HP:0003128 ICD10CM:E87.2 SNOMEDCT:91273001 RGO:30196 lactic acidosis RGO:30196 HP:0040010 RGO:30198 small posterior fossa RGO:30198 HP:0001601 SNOMEDCT:38086007 RGO:30203 laryngomalacia RGO:30203 RGO:30205 optic nerve meningocele RGO:30205 RGO:30206 opalescent/rootless teeth RGO:30206 RGO:30207 large sella RGO:30207 RGO:30208 V-shaped sella turcica RGO:30208 RGO:30218 brachydactyly of fingers and toes RGO:30218 SNOMEDCT:396275006 RGO:30219 degenerative arthropathy RGO:30219 RGO:30222 multiple malformations of the vertebrae and ribs RGO:30222 RGO:30225 chromosome dup(4p) syndrome RGO:30225 RGO:30226 ankle synovial chondromatosis RGO:30226 RGO:30227 metaphyseal undermodeling RGO:30227 RGO:30228 skull base overgrowth RGO:30228 RGO:30229 spondylar dysplasia RGO:30229 RGO:30231 skeletal maturation of phalanges before carpals RGO:30231 RGO:30232 lethal congenital dwarfism RGO:30232 RGO:30233 generalized skeletal sclerosis RGO:30233 RGO:30234 accelerated bone maturation RGO:30234 RGO:30237 widened triradiate cartilage RGO:30237 RGO:30238 irregular acetabula RGO:30238 RGO:30240 notched iliac wings RGO:30240 RGO:30241 delayed ossification of femoral heads RGO:30241 RGO:30244 premature fusion of the sternal ossification centers RGO:30244 RGO:30246 spontaneous sternal fracture RGO:30246 RGO:30247 sternal insufficiency fracture RGO:30247 RGO:30249 unilateral rib notching RGO:30249 AO2 McAlister dysplasia atelosteogenesis de la Chapelle type de la Chapelle dysplasia neonatal osseous dysplasia 1 ORDO:56304 SNOMEDCT:254055004 RGO:30253 atelosteogenesis type 2 RGO:30253 HP:0001057 SNOMEDCT:35484002 RGO:30255 cutis aplasia RGO:30255 RGO:30257 right bundle branch block plus RGO:30257 RGO:30258 progressive myopathy RGO:30258 RGO:30259 multiple Noonan-like anomalies RGO:30259 HP:0000078 RGO:30262 genital anomalies RGO:30262 RGO:30263 craniofacial anomalies RGO:30263 HP:0002217 RGO:30264 slow-growing hair RGO:30264 ORDO:1084 ORDO:2148 RGO:30272 type 1 lissencephaly syndrome RGO:30272 RGO:30273 type 2 lissencephaly syndrome RGO:30273 RGO:30274 type 3 lissencephaly syndrome RGO:30274 MEB disease muscle-eye-brain disease RGO:30275 cerebro-oculo-muscular syndrome RGO:30275 DOID:0050453 HP:0001339 RGO:30276 isolated lissencephaly syndrome RGO:30276 RGO:30277 cerebro-cerebellar lissenencephaly syndrome RGO:30277 RGO:30280 sex chromosome abnormality RGO:30280 DOID:2338 SNOMEDCT:126551000 RGO:30281 neoplasm of mandible RGO:30281 RGO:30282 trichodystrophy RGO:30282 HP:0010105 RGO:30285 short first metatarsal RGO:30285 RGO:30287 Fukuyama syndrome RGO:30287 RGO:30292 paravertebral calcification RGO:30292 RGO:30294 abnormally shaped metacarpals and phalanges RGO:30294 RGO:30296 second metatarsal syndrome RGO:30296 RGO:30297 long second MC RGO:30297 RGO:30299 finger contractions RGO:30299 RGO:30300 Meunke FGFR3 mutation-craniosynostosis RGO:30300 RGO:30301 carpal-tarsal coalition RGO:30301 HP:0001762 RGO:30303 clubfeet RGO:30303 HP:0009803 RGO:30305 short phalanges RGO:30305 RGO:30306 glutaric aciduria type 1 RGO:30306 SNOMEDCT:328383001 RGO:30308 chronic liver disease RGO:30308 RGO:30309 demyelination of the corpus callosum RGO:30309 RGO:30310 chronic severe alcoholism RGO:30310 HP:0001985 RGO:30311 hypoketotic hypoglycemia RGO:30311 DOID:14701 HP:0003353 SNOMEDCT:69080001 RGO:30312 propionyl-CoA carboxylase deficiency RGO:30312 HP:0005979 RGO:30313 metabolic ketoacidosis RGO:30313 RGO:30314 acute basal ganglia infarction RGO:30314 RGO:30315 T2-bright periventricular tissue RGO:30315 SNOMEDCT:204044008 RGO:30316 aplasia of corpus callosum RGO:30316 RGO:30318 kyphoscoliosis syndrome RGO:30318 RGO:30319 leukoencephaly RGO:30319 RGO:30320 bone marrow/skin/hair abnormalities RGO:30320 RGO:30321 biomechanical stress RGO:30321 RGO:30322 guitar playing RGO:30322 RGO:30323 clublike femur RGO:30323 RGO:30324 clublike humerus RGO:30324 RGO:30325 long 2nd metacarpal RGO:30325 RGO:30326 long 5th metacarpal RGO:30326 RGO:30332 polycystic renal dysplasia RGO:30332 RGO:30333 finger flexion deformities RGO:30333 RGO:30334 pigmented skin patches RGO:30334 HP:0000924 RGO:30335 skeletal abnormalities RGO:30335 RGO:30336 facial anomalies RGO:30336 HP:0011968 ICD10CM:R63.3 RGO:30337 feeding difficulties RGO:30337 HP:0007902 ICD10CM:H43.1 SNOMEDCT:31341008 RGO:30338 vitreous hemorrhage RGO:30338 RGO:30339 absent carotid artery RGO:30339 RGO:30341 myositis ossificans of extraocular muscles RGO:30341 DOID:3612 RADLEX:RID3549 SNOMEDCT:399463004 RGO:30342 retinitis RGO:30342 RGO:30343 retinal fibrosis RGO:30343 RGO:30345 orbital metastasis RGO:30345 RGO:30347 discontinuous eyebrow RGO:30347 RGO:30349 absent outer half of eyebrows RGO:30349 RGO:30350 lateral extension of eyebrows RGO:30350 RGO:30351 prematurely gray eyebrows RGO:30351 RGO:30352 redundant eyebrows RGO:30352 RGO:30353 fine eyebrows RGO:30353 RGO:30354 bitemporal eyebrows RGO:30354 HP:0009927 SNOMEDCT:111317000 RGO:30358 absent nose RGO:30358 RGO:30360 benign enlargement of the subarachnoid space RGO:30360 RGO:30361 contralateral hemiparesis in some RGO:30361 RGO:30362 unilateral megalencephaly RGO:30362 RGO:30364 generalized edema at birth RGO:30364 RGO:30365 flexion contracture of the feet RGO:30365 HP:0002448 RGO:30367 progressive encephalopathy RGO:30367 RGO:30370 absent olfactory tracts and bulb RGO:30370 RGO:30371 thumb duplication RGO:30371 RGO:30372 abnormal metacarpals and metatarsals RGO:30372 RGO:30373 familial basilar invagination RGO:30373 Bull-Nixon syndrome primary basilar impression ORDO:2285 RGO:30374 familial primary basilar impression RGO:30374 RGO:30377 pigmented nevi and freckles RGO:30377 RGO:30379 insulin-dependent diabetes RGO:30379 RGO:30381 radio-ulnar synostosis RGO:30381 RGO:30383 fusion of the cuboid and third cuneiform bones RGO:30383 RGO:30384 proximally placed thumbs and great toes RGO:30384 RGO:30385 short fifth fingers with clinodactyly RGO:30385 RGO:30386 syndactyly of the fourth and fifth toes RGO:30386 RGO:30387 hearing deficit RGO:30387 HP:0011326 RGO:30388 coronal synostosis RGO:30388 RGO:30389 variable finding RGO:30389 HP:0009944 SNOMEDCT:51219000 RGO:30392 bifid thumb RGO:30392 HP:0001545 RGO:30393 anteriorly placed anus RGO:30393 RGO:30394 unilateral ulnar aplasia RGO:30394 RGO:30395 unilateral microphthalmia RGO:30395 RGO:30396 polydactyly of the feet RGO:30396 RGO:30398 sparse curly hair RGO:30398 HP:0005773 RGO:30399 short forearm RGO:30399 RGO:30400 fused elbow RGO:30400 RGO:30401 finger anomaly RGO:30401 RGO:30402 hyperostosis of frontal and vertex regions RGO:30402 HP:0001140 RGO:30403 epibulbar dermoids RGO:30403 RGO:30404 epibulbar nevus RGO:30404 HP:0001263 SNOMEDCT:248290002 RGO:30405 developmental delay RGO:30405 RGO:30406 hip osteochondritis RGO:30406 HP:0001770 RGO:30407 toe syndactyly RGO:30407 RGO:30409 gigantism at birth RGO:30409 RGO:30410 rudimentary auricle RGO:30410 RGO:30411 silver hair RGO:30411 RGO:30412 neurologic abnormality RGO:30412 RGO:30413 Meunke FGFR3 mutation RGO:30413 HP:0004442 RGO:30414 sagittal suture synostosis RGO:30414 RGO:30415 anterior dislocation of tibia RGO:30415 HP:0011330 RGO:30416 metopic synostosis RGO:30416 RGO:30417 S-curved lower lids RGO:30417 RGO:30418 slender bones RGO:30418 DOID:9370 HP:0000520 SNOMEDCT:18265008 RGO:30419 proptosis RGO:30419 RGO:30420 chemotactic defect RGO:30420 SNOMEDCT:109417006 RGO:30421 lambdoid craniosynostosis RGO:30421 RGO:30425 rib agenesis RGO:30425 HP:0000773 RGO:30426 rib hypoplasia RGO:30426 HP:0000448 SNOMEDCT:249311009 RGO:30430 large nose RGO:30430 HP:0000154 RGO:30431 large mouth RGO:30431 RGO:30432 broad and short distal phalanges RGO:30432 brachydactyly-clinodactyly DOID:0110966 RGO:30435 brachydactyly type A3 RGO:30435 RGO:30439 muscular hypoplasia RGO:30439 HP:0000365 SNOMEDCT:95828007 RGO:30440 congenital deafness RGO:30440 RGO:30443 slow growth of nails RGO:30443 RGO:30444 congenital universal alopecia RGO:30444 RGO:30446 leg ulcers RGO:30446 HP:0001908 SNOMEDCT:41614006 RGO:30447 hypoplastic anemia RGO:30447 RGO:30448 radio-ulnar defects RGO:30448 RGO:30449 radioulnar defects RGO:30449 RGO:30451 cutaneomeningeospinal angiomatosis RGO:30451 HP:0025520 ICD10CM:L94.2 SNOMEDCT:21323007 RGO:30453 calcinosis cutis RGO:30453 RGO:30454 auricular tags RGO:30454 RGO:30455 gingival tags RGO:30455 RGO:30456 anal tags RGO:30456 RGO:30457 ear malformation RGO:30457 RGO:30458 prematurely white hair RGO:30458 HP:0001371 RGO:30460 contractures RGO:30460 RGO:30461 trigeminal anesthesia RGO:30461 RGO:30462 ear deformities RGO:30462 DOID:2583 HP:0004313 SNOMEDCT:119250001 RGO:30465 hypogammaglobulinemia RGO:30465 HP:0002750 RGO:30466 skeletal maturation retardation RGO:30466 RGO:30467 partial or complete absence of nails RGO:30467 RGO:30468 variable absence of phalanges and carpal and tarsal bones RGO:30468 RGO:30469 flexion and extension deformities of hands RGO:30469 RGO:30470 claw toes RGO:30470 RGO:30471 loose skin of neck, hands and feet RGO:30471 RGO:30472 perioral and nasal papillomata RGO:30472 HP:0002212 SNOMEDCT:225570000 RGO:30473 curly hair RGO:30473 RGO:30474 bilateral cryptomicrotia RGO:30474 HP:0001800 RGO:30475 hypoplastic toenails RGO:30475 RGO:30476 vitreo-retinal degeneration RGO:30476 HP:0011003 SNOMEDCT:34187009 RGO:30477 high myopia RGO:30477 RGO:30478 occipital scalp defect RGO:30478 HP:0002990 RGO:30479 fibular aplasia RGO:30479 HP:0001519 RGO:30480 marfanoid habitus RGO:30480 RGO:30481 blepharonasofacial anomaly RGO:30481 RGO:30482 coup-de-sabre defect RGO:30482 RGO:30483 retinal pigmentary dystrophy RGO:30483 DOID:0050591 HP:0000677 ICD10CM:K00.0 ORDO:99798 SNOMEDCT:64969001 RGO:30484 oligodontia RGO:30484 RGO:30486 immune abnormalities RGO:30486 ORDO:1987 RGO:30489 femoral hypoplasia or aplasia RGO:30489 RGO:30491 defects in the ulnar ray RGO:30491 RGO:30492 femur aplasia RGO:30492 RGO:30493 femur hypoplasia RGO:30493 RGO:30494 upper extremity anomaly RGO:30494 complete absence of a limb HP:0009827 SNOMEDCT:62588002 RGO:30495 amelia RGO:30495 HP:0009828 RGO:30496 peromelia RGO:30496 RGO:30497 ulnar defect RGO:30497 HP:0001373 RGO:30498 joint dislocation RGO:30498 HP:0007020 RGO:30500 progressive spastic paraplegia RGO:30500 HP:0001260 SNOMEDCT:8011004 RGO:30501 dysarthria RGO:30501 RGO:30502 pigmented cutaneous nevi RGO:30502 RGO:30505 fused elbows RGO:30505 RGO:30506 progressive emaciation RGO:30506 RGO:30507 nodular erythema RGO:30507 HP:0001176 RGO:30508 large hands RGO:30508 RGO:30509 thick fingers RGO:30509 RGO:30510 intrauterine growth acceleration RGO:30510 HP:0001263 RGO:30511 mental and motor retardation RGO:30511 RGO:30512 contracture of the feet RGO:30512 HP:0004419 RGO:30514 recurrent thrombophlebitis RGO:30514 RGO:30516 wasting of the hand muscles RGO:30516 SNOMEDCT:239881008 RGO:30519 Otto pelvis RGO:30519 RGO:30520 narrow lumbar canal RGO:30520 RGO:30521 multiple arterial occlusions RGO:30521 DOID:0060673 HP:0000659 ORDO:708 SNOMEDCT:204153003 RGO:30522 Peters anomaly RGO:30522 RGO:30523 variable iridolenticulocorneal adhesions RGO:30523 SNOMEDCT:66123000 RGO:30528 tongue ulceration RGO:30528 HP:0009778 RGO:30529 hypoplastic thumbs RGO:30529 RGO:30530 single upper incisor RGO:30530 HP:0001000 RGO:30531 abnormal skin pigmentation RGO:30531 HP:0000612 RGO:30532 coloboma of the iris RGO:30532 SNOMEDCT:205828009 RGO:30534 Biemond syndrome RGO:30534 RGO:30535 familial imperforate anus-cleft lip-coloboma RGO:30535 HP:0000105 SNOMEDCT:300444006 RGO:30536 nephromegaly RGO:30536 RGO:30537 pulmonary cysts RGO:30537 RGO:30538 multifocal cystic hamartoma of the lung RGO:30538 RGO:30539 parenchymal overgrowth of the kidney RGO:30539 HP:0030053 RGO:30540 indurated skin RGO:30540 RGO:30541 limited joint movement RGO:30541 HP:0000260 RGO:30542 large anterior fontanelle RGO:30542 HP:0001263 RGO:30543 psychomotor delay RGO:30543 RGO:30544 short fingers and toes RGO:30544 RGO:30545 stubby broad thumbs and halluces RGO:30545 RGO:30547 bitemporal scarlike skin defects RGO:30547 RGO:30548 multiple rows of upper eyelashes RGO:30548 DOID:8541 ORDO:3162 SNOMEDCT:4950009 RGO:30554 Sézary syndrome RGO:30554 RGO:30556 progressive generalized hyperpigmentation RGO:30556 RGO:30558 lentigines RGO:30558 RGO:30559 mucocutaneous myxoma RGO:30559 RGO:30560 blue nevi RGO:30560 RGO:30562 trichomegaly RGO:30562 HP:0004059 RGO:30563 radial dysplasia RGO:30563 RGO:30564 postaxial ulnar deficiency RGO:30564 RGO:30565 postaxial fibular deficiency RGO:30565 HP:0011220 RGO:30566 prominent forehead RGO:30566 RGO:30567 hypoplastic vermis RGO:30567 RGO:30568 atrial or atrioventricular septal defect RGO:30568 ORDO:90646 RGO:30569 X-linked deafness and hypogonadism RGO:30569 RGO:30572 prolonged QT syndrome RGO:30572 HP:0100662 SNOMEDCT:46176001 RGO:30573 chondritis RGO:30573 SNOMEDCT:37600001 RGO:30574 perichondritis RGO:30574 HP:0000706 RGO:30575 pseudoanodontia RGO:30575 RGO:30576 autonomic nerve disorder RGO:30576 RGO:30577 loss of thermoregulation RGO:30577 RGO:30578 unilateral flushing RGO:30578 RGO:30579 unilateral perspiration RGO:30579 RGO:30581 high cervical encephalocele RGO:30581 RGO:30582 thoracic meningocele RGO:30582 RGO:30583 familial hidrotic ectodermal dysplasia RGO:30583 RGO:30584 familial idiopathic symmetric basal ganglia calcification and microcephaly RGO:30584 RGO:30585 infantile familial encephalopathy with cerebral calcification and leukodystrophy RGO:30585 RGO:30586 leptomeningeal hamartoma RGO:30586 RGO:30587 chondrocyte inclusions RGO:30587 RGO:30588 idiopathic fetal encephalopathy RGO:30588 RGO:30589 hypoxia-ischemia RGO:30589 RGO:30590 lipomembranous polycystic osteodysplasia RGO:30590 DOID:182 HP:0003761 SNOMEDCT:6595006 RGO:30591 calcinosis RGO:30591 RGO:30592 Prader-Willi phenotype RGO:30592 RGO:30594 large septum pellucidum RGO:30594 RGO:30595 costovertebral anomaly RGO:30595 RGO:30597 L1CAM mutation RGO:30597 RGO:30598 cavum septi pellucidi abscess RGO:30598 RGO:30599 expanding cavum septi pellucidi cyst RGO:30599 HP:0006789 RGO:30600 mitochondrial encephalopathy RGO:30600 RGO:30602 clinodactyly of 2nd digit RGO:30602 RGO:30603 clinodactyly of 5th digit RGO:30603 ORDO:939 SNOMEDCT:237957007 RGO:30605 3-hydroxyisobutyric aciduria RGO:30605 DOID:14723 SNOMEDCT:124258007 RGO:30606 3-ketothiolase deficiency RGO:30606 SNOMEDCT:276721005 RGO:30607 cerebral dysgenesis RGO:30607 RGO:30609 glutaric acidemia type 1 RGO:30609 DOID:0060358 ORDO:26791 RGO:30610 glutaric acidemia type 2 RGO:30610 RGO:30612 familial schizencephaly RGO:30612 DOID:471 RGO:30614 skin hemangioma RGO:30614 RGO:30615 intracranial malformation RGO:30615 RGO:30616 carotid-vertebral hypoplasia RGO:30616 ORDO:99810 RGO:30617 familial porencephaly RGO:30617 RGO:30619 familial coxa vara RGO:30619 RGO:30622 mild platyspondyly with end-plate concavity RGO:30622 RGO:30623 conduction defect RGO:30623 RGO:30625 cerebellar vermis dysplasia RGO:30625 RGO:30626 incomplete periventricular myelination RGO:30626 RGO:30627 autosomal dominant vermis hypoplasia RGO:30627 RGO:30628 X-linked vermis hypoplasia RGO:30628 RGO:30629 unilateral cerebellar hemisphere atrophy RGO:30629 RGO:30630 agenesis of the caudate nucleus RGO:30630 RGO:30632 endosteal sclerosis RGO:30632 RGO:30633 repeated infections RGO:30633 RGO:30635 ocular abnormality RGO:30635 RGO:30636 general signs of inflammation and secondary amyloidosis RGO:30636 RGO:30637 general signs of inflammation RGO:30637 RGO:30638 limb anomaly RGO:30638 RGO:30639 erythroid macrocytosis RGO:30639 RGO:30640 megaloblastic marrow RGO:30640 RGO:30641 external ear deformity RGO:30641 RGO:30642 aplasia or hypoplasia of fibulas RGO:30642 ICD10CM:Q04.1 RADLEX:RID34733 RGO:30644 arhinencephaly RGO:30644 DOID:10140 HP:0001097 ICD10CM:H04.12 SNOMEDCT:46152009 RGO:30645 dry eye syndrome RGO:30645 RGO:30647 distinctive facial dysmorphology RGO:30647 HP:0003764 RGO:30648 multiple nevi RGO:30648 RGO:30650 homozygous achondroplasia RGO:30650 RGO:30652 syndactyly of fingers and toes RGO:30652 RGO:30655 severely short ulna RGO:30655 RGO:30656 severely short radius RGO:30656 HP:0009701 RGO:30657 metacarpal synostosis RGO:30657 RGO:30658 phalangeal deformity RGO:30658 ORDO:1439 RGO:30659 ring chromosome 12 RGO:30659 UPD 7 RGO:30661 uniparental disomy 7 RGO:30661 UPD RGO:30662 uniparental disomy RGO:30662 RGO:30666 congenital hypertrichosis universalis RGO:30666 SNOMEDCT:387467008 RGO:30667 cyclosporin RGO:30667 DOID:8741 HP:0001051 SNOMEDCT:86708008 RGO:30670 seborrhea RGO:30670 DOID:6543 HP:0001061 ICD10CM:L70 SNOMEDCT:11381005 RGO:30671 acne RGO:30671 SNOMEDCT:63398001 RGO:30678 pseudomonas infection RGO:30678 HP:0040185 RGO:30680 macrothrombocytopenia RGO:30680 SNOMEDCT:90708001 RGO:30682 renal disease RGO:30682 RGO:30683 multiple neural tube defects RGO:30683 RGO:30686 nodulosis RGO:30686 RGO:30687 manual labor RGO:30687 RGO:30688 athletic activity RGO:30688 RGO:30690 chromosome 14 disorder RGO:30690 RGO:30691 chromosome 7 disorder RGO:30691 RGO:30692 chromosome 18p- disorder RGO:30692 RGO:30693 chromosome 7q- disorder RGO:30693 SNOMEDCT:109493006 RGO:30694 radicular dentine dysplasia RGO:30694 RGO:30695 sclerotic long bones RGO:30695 RGO:30696 sclerotic mandible RGO:30696 RGO:30697 sclerotic maxilla RGO:30697 RGO:30698 narrow marrow space RGO:30698 RGO:30699 pseudodistichiasis RGO:30699 HP:0007754 SNOMEDCT:276436007 RGO:30700 macular dystrophy RGO:30700 SNOMEDCT:33076008 RGO:30702 hemimelia RGO:30702 HP:0002211 SNOMEDCT:247564004 RGO:30706 white forelock RGO:30706 RGO:30707 hypopigmentation of the central portion of the forehead RGO:30707 RGO:30708 hypopigmentation of the chin RGO:30708 gracile ribs slender ribs HP:0000883 RGO:30709 thin ribs RGO:30709 twisted ribs HP:0010561 RGO:30710 wavy ribs RGO:30710 HP:0003311 RGO:30716 odontoid hypoplasia RGO:30716 RGO:30717 odontoid aplasia RGO:30717 RGO:30718 presacral ependymoma RGO:30718 RGO:30719 tailgut cyst RGO:30719 RGO:30721 idiopathic spinal canal widening RGO:30721 HP:0004912 RGO:30723 hypophosphatemic rickets RGO:30723 RGO:30725 anomalous position of the gallbladder RGO:30725 RGO:30726 chronic stress RGO:30726 RGO:30728 basal cell carcinoma/nevi RGO:30728 DOID:11155 HP:0000966 ICD10CM:L74.4 SNOMEDCT:45004005 RGO:30729 hypohidrosis RGO:30729 SNOMEDCT:37200009 RGO:30730 disorder of tyrosine metabolism RGO:30730 DOID:0050758 HP:0001942 ICD10CM:E87.2 SNOMEDCT:59455009 RGO:30731 metabolic acidosis RGO:30731 RGO:30735 familial Chiari malformation type I RGO:30735 RGO:30736 cranial radiation RGO:30736 RGO:30737 intrathecal methotrexate sodium treatment RGO:30737 HP:0002102 RADLEX:RID3540 SNOMEDCT:196075003 RGO:30738 pleuritis RGO:30738 RGO:30739 ectopic chorionic gonadotropin-producing tumor RGO:30739 RGO:30740 involutional gynecomastia RGO:30740 SNOMEDCT:237451004 RGO:30741 pubertal gynecomastia RGO:30741 RGO:30742 physiologic neonatal gynecomastia RGO:30742 Dilantin SNOMEDCT:387220006 SNOMEDCT:40556005 RGO:30745 phenytoin RGO:30745 RGO:30746 antiandrogen medication RGO:30746 SNOMEDCT:22672005 SNOMEDCT:703842006 RGO:30747 amphetamine RGO:30747 RGO:30748 marijuana use RGO:30748 RGO:30749 heroin use RGO:30749 RGO:30750 antiulcer medication RGO:30750 RGO:30751 cancer chemotherapy RGO:30751 RGO:30752 cardiovascular medication RGO:30752 RGO:30753 psychoactive agent RGO:30753 Engelmann disease diaphyseal dysplasia Camurati-Engelmann diaphyseal dysplasia Engelmann type hereditary multiple diaphyseal sclerosis progressive diaphyseal dysplasia ribbing disease DOID:4997 ORDO:1328 RGO:30755 Camurati-Engelmann disease RGO:30755 RGO:30756 acromesomelic dysplasia Campailla-Martinelli type RGO:30756 acromesomelic dysplasia type Maroteaux ORDO:40 RGO:30757 acromesomelic dysplasia Maroteaux type RGO:30757 HP:0003510 RGO:30759 dwarfism RGO:30759 RGO:30760 corneal dysplasia RGO:30760 RGO:30761 pre-pubertal normal variant RGO:30761 RGO:30762 hip surgery RGO:30762 RGO:30763 medial dislocation of femoral component of total hip arthroplasty RGO:30763 ICD10CM:L70.1 SNOMEDCT:42228007 RGO:30764 acne conglobata RGO:30764 suppurative hidradenitis DOID:2280 HP:0040154 ICD10CM:L73.2 SNOMEDCT:59393003 RGO:30765 hidradenitis suppurativa RGO:30765 hypophosphatemic rickets X-linked dominant DOID:0050445 SNOMEDCT:82236004 RGO:30766 X-linked hypophosphatemic rickets RGO:30766 RGO:30767 sacral duplication RGO:30767 HP:0100562 SNOMEDCT:360527003 RGO:30768 diplomyelia RGO:30768 RGO:30769 severe fixed retroflexion of the head RGO:30769 HP:0000470 SNOMEDCT:95427009 RGO:30770 short neck RGO:30770 RGO:30771 immobile neck RGO:30771 spondylocostal dysostosis - anal and genitourinary malformations RGO:30772 Casamassima-Morton-Nance syndrome RGO:30772 RADLEX:RID35616 SNOMEDCT:27173008 RGO:30774 tarsal coalition RGO:30774 heel spur DOID:210 ICD10CM:M77.3 SNOMEDCT:55260003 RGO:30775 calcaneal spur RGO:30775 RGO:30777 bumps on the head RGO:30777 Langer-Giedion syndrome trichorhinophalangeal syndrome type 2 RGO:30778 trichorhinophalangeal dysplasia type 2 RGO:30778 RGO:30779 femoral thigh spur RGO:30779 HP:0030359 RGO:30780 squamous cell lung carcinoma RGO:30780 HP:0030357 RGO:30781 small cell lung carcinoma RGO:30781 DOID:14484 ICD10CM:B42 ORDO:826 SNOMEDCT:42094007 RGO:30783 sporotrichosis RGO:30783 RGO:30784 acquired thymic cyst RGO:30784 RGO:30785 congenital thymic cyst RGO:30785 SNOMEDCT:253166000 RGO:30786 lateral meningocele RGO:30786 SNOMEDCT:63697000 RGO:30787 cardiopulmonary bypass RGO:30787 SNOMEDCT:2598006 RGO:30788 open heart surgery RGO:30788 RGO:30789 thoracic trauma RGO:30789 SNOMEDCT:41110003 RGO:30791 blast injury RGO:30791 RGO:30793 aspirated food RGO:30793 DOID:9398 RADLEX:RID3438 SNOMEDCT:80384002 RGO:30794 epiglottitis RGO:30794 RGO:30795 hanging RGO:30795 SNOMEDCT:66466001 RGO:30796 suffocation RGO:30796 RGO:30797 agonal breathing RGO:30797 SNOMEDCT:300936002 RGO:30798 terminal illness RGO:30798 RGO:30799 head trauma RGO:30799 RGO:30800 unilateral ductus shunt RGO:30800 RGO:30801 atypical pulmonary edema RGO:30801 RGO:30802 limb/pelvis hypoplasia/aplasia RGO:30802 HP:0001362 RGO:30803 skull defect RGO:30803 RGO:30805 Michel dysplasia RGO:30805 RGO:30806 Michel aplasia RGO:30806 HP:0011372 RGO:30807 aplasia of the inner ear RGO:30807 RGO:30808 dysplasia of the inner ear RGO:30808 RGO:30809 cochleopathy RGO:30809 RGO:30810 postauricular tags RGO:30810 HP:0100277 RGO:30811 periauricular pits RGO:30811 RGO:30812 periauricular tag RGO:30812 SNOMEDCT:205648000 RGO:30813 trisomy 7 RGO:30813 HP:0001822 SNOMEDCT:122480009 RGO:30815 hallux valgus RGO:30815 HP:0000211 SNOMEDCT:87866006 RGO:30816 trismus RGO:30816 peculiar facies unusual facies HP:0001999 SNOMEDCT:398302004 RGO:30817 facial dysmorphism RGO:30817 RGO:30818 humero-scapular synostosis RGO:30818 HP:0000078 RGO:30819 genital abnormality RGO:30819 RGO:30820 mirror hands and feet RGO:30820 RGO:30821 grooves in the alae nasi and columella with incomplete fusion of the external nares RGO:30821 RGO:30822 syndactyyl RGO:30822 RGO:30824 duplication of the ulna RGO:30824 RGO:30825 duplication of the fibula RGO:30825 RGO:30826 duplication of the tarsal bones RGO:30826 SNOMEDCT:397734008 RGO:30834 acrodystrophic neuropathy RGO:30834 SNOMEDCT:27831002 RGO:30835 snake venom RGO:30835 RGO:30836 scorpion sting RGO:30836 RGO:30840 gastrointestinal abnormality RGO:30840 HP:0003037 RGO:30842 enlarged joints RGO:30842 HP:0003026 RGO:30843 short tubular bones RGO:30843 RGO:30847 sellar lesion RGO:30847 RGO:30848 parasellar lesion RGO:30848 RGO:30849 foramen of Monro lesion RGO:30849 RGO:30852 nasopharyngeal lesion RGO:30852 RGO:30853 infratemporal fossa lesion RGO:30853 RGO:30854 sinonasal lesion RGO:30854 RGO:30856 multiple dentigerous cysts RGO:30856 HP:0001822 ICD10CM:M21.61 SNOMEDCT:415692008 RGO:30859 bunion RGO:30859 RGO:30860 bursal fluid collection RGO:30860 RADLEX:RID3915 RGO:30861 meniscal cyst RGO:30861 RGO:30863 localized nodular synovitis RGO:30863 RGO:30864 parosteal chondrosarcoma RGO:30864 RGO:30865 articular chondroma RGO:30865 RGO:30866 para-articular chondroma RGO:30866 RGO:30867 juxtaarticular myxoma RGO:30867 RGO:30868 soft-tissue chondroma RGO:30868 RADLEX:RID13399 RGO:30869 synovial bursa RGO:30869 RGO:30870 synovial ganglion RGO:30870 HP:0009594 RGO:30871 retinal hamartoma RGO:30871 RGO:30873 small ascending aorta RGO:30873 RGO:30874 small aortic arch RGO:30874 RGO:30875 large ascending aorta RGO:30875 RGO:30876 large aortic arch RGO:30876 RGO:30877 ischemia of digits RGO:30877 RGO:30879 tunica albuginea ossification RGO:30879 RGO:30880 acromial spur RGO:30880 RGO:30881 lateral frontal horn RGO:30881 RGO:30882 pelvic venous spur RGO:30882 RGO:30883 iliac horn RGO:30883 RGO:30884 spur in the midportion of the long bones RGO:30884 RGO:30885 Bowdler spur RGO:30885 RGO:30886 skull protuberance RGO:30886 RGO:30887 tortuous vertebral artery RGO:30887 RGO:30888 bony dysplasia RGO:30888 RGO:30889 idiopathic dural ectasia RGO:30889 RGO:30890 atherosclerosis of ophthalmic artery RGO:30890 RGO:30891 atherosclerosis of internal carotid artery RGO:30891 RGO:30892 intraocular infection RGO:30892 RGO:30893 intraocular abscess RGO:30893 RGO:30894 bacterial ophthalmitis RGO:30894 RGO:30895 Michelin tire baby syndrome RGO:30895 RGO:30898 debilitating disease RGO:30898 DOID:876 ORDO:764 SNOMEDCT:65110003 RGO:30899 pyomyositis RGO:30899 SNOMEDCT:125643001 SNOMEDCT:59091005 RGO:30900 open wound RGO:30900 SNOMEDCT:113154008 RGO:30901 hypodermoclysis RGO:30901 HP:0030056 RGO:30903 uncombable hair RGO:30903 HP:0007495 RGO:30905 prematurely aged appearance RGO:30905 RGO:30906 tall and thin stature RGO:30906 HP:0002209 RGO:30907 thin scalp hair RGO:30907 HP:0000520 RGO:30908 prominent eyes RGO:30908 HP:0000444 RGO:30909 beaked nose RGO:30909 RGO:30910 mottled skin hyperpigmentation RGO:30910 RGO:30911 skin atrophy on limbs RGO:30911 HP:0007485 RGO:30912 absence of subcutaneous fat RGO:30912 RGO:30913 early atherosclerosis RGO:30913 RGO:30914 early onset of diabetes mellitus RGO:30914 RGO:30915 dystrophic calcinosis RGO:30915 RGO:30916 familial osteoma cutis RGO:30916 RGO:30918 multiple miliary osteoma of the face RGO:30918 HP:0100246 RGO:30919 isolated osteoma RGO:30919 RGO:30920 widespread osteoma RGO:30920 RGO:30921 platelike osteoma RGO:30921 RGO:30924 cutaneous nevi RGO:30924 SNOMEDCT:95501007 RGO:30925 retinal arteriovenous malformation RGO:30925 RGO:30926 central venous catheterization RGO:30926 RGO:30927 pulmonary artery catheterization RGO:30927 RGO:30928 myocardial perforation RGO:30928 RGO:30929 FGFR-opaty RGO:30929 RGO:30930 cardiomegaly in childhood RGO:30930 RGO:30931 heart failure in childhood RGO:30931 RGO:30932 early cementoma RGO:30932 SNOMEDCT:125299007 RGO:30933 calcified thrombus RGO:30933 RADLEX:RID3366 SNOMEDCT:12856003 RGO:30934 varicose vein RGO:30934 RGO:30935 widespread bone metastases RGO:30935 RGO:30936 high body weight RGO:30936 RGO:30937 soft-tissue infection RGO:30937 RGO:30938 muscle tumor RGO:30938 RGO:30939 lymph node excision RGO:30939 SNOMEDCT:12167004 RGO:30940 lymphocyst RGO:30940 ORDO:99756 RGO:30941 alveolar-type rhabdomyosarcoma RGO:30941 RGO:30942 hypertrophic osteoarthritis RGO:30942 RGO:30943 chronic trauma RGO:30943 RADLEX:RID4778 SNOMEDCT:26396009 RGO:30944 subluxation RGO:30944 RGO:30945 athletic activity in adolescence RGO:30945 RGO:30946 prior arthritis RGO:30946 RGO:30948 osteochondral fragment RGO:30948 intra-articular osteochondral fragment RGO:30949 joint mouse RGO:30949 RGO:30950 chronic rheumatoid arthritis RGO:30950 RGO:30951 detached osteochondral fragment RGO:30951 SNOMEDCT:4857006 RGO:30952 sequestrum RGO:30952 RGO:30953 parosteal ostesarcoma RGO:30953 RGO:30955 Pellegrini-Stieda disease RGO:30955 RGO:30956 avulsed fracture fragment RGO:30956 RGO:30957 calcified meniscal fragment RGO:30957 RGO:30958 calcific synovitis RGO:30958 RGO:30959 intra-articular calcification RGO:30959 RGO:30961 inflammatory synovitis RGO:30961 RGO:30962 crystal synovitis RGO:30962 RADLEX:RID3637 SNOMEDCT:431901000124100 RGO:30963 infectious synovitis RGO:30963 HP:0030038 RADLEX:RID4128 SNOMEDCT:31186001 SNOMEDCT:423699002 RGO:30964 enchondroma RGO:30964 RGO:30967 synovial-type lymphangiomatosis RGO:30967 RGO:30968 synovial-type hemangiomatosis RGO:30968 RGO:30969 degenerative arthritic cyst RGO:30969 RGO:30970 gouty erosion RGO:30970 RADLEX:RID3894 RGO:30971 geode RGO:30971 RGO:30972 rheumatoid erosion RGO:30972 RGO:30973 neuropathic erosion RGO:30973 RGO:30974 psoriatic erosion RGO:30974 RGO:30979 plasma cell dyscrasia RGO:30979 RGO:30985 cis-retinoic acid RGO:30985 RGO:30986 vitamin D-resistant rickets treatment RGO:30986 RGO:30987 low-grade chondrosarcoma RGO:30987 SNOMEDCT:22780006 RGO:30988 subperiosteal hemorrhage RGO:30988 RGO:30990 exostosis of medial tibial condyle RGO:30990 RGO:30992 intracapsular osteochondroma RGO:30992 SNOMEDCT:446593006 SNOMEDCT:703696007 RGO:30993 bizarre parosteal osteochondromatous proliferation RGO:30993 RGO:30994 traction exostosis RGO:30994 RGO:30995 cranioectodermal dysplasia and bone dysplasia RGO:30995 HP:0012531 RADLEX:RID28803 SNOMEDCT:22253000 RGO:30996 pain RGO:30996 HP:0010783 SNOMEDCT:247441003 SNOMEDCT:70819003 RGO:30997 erythema RGO:30997 RGO:30998 periosteal reaction of the tubular bones of hands and feet RGO:30998 RGO:30999 soft tissue calcification RGO:30999 RGO:31000 periosteal hyperostosis RGO:31000 RGO:31001 thyroid acropathy RGO:31001 RGO:31002 treated hyperparathyroidism RGO:31002 HP:0003417 RGO:31004 coronal clefts RGO:31004 hyperostosis corticalis generalisata DOID:0080034 RGO:31005 endosteal hyperostosis RGO:31005 RGO:31006 sclerosis of jaw bone RGO:31006 RGO:31008 healing osteomalacia RGO:31008 RGO:31009 idiopathic hypertrophic osteoarthropathy RGO:31009 RGO:31010 dense skull base RGO:31010 RGO:31011 dense facial bones RGO:31011 RGO:31012 diaphyseal medullary stenosis RGO:31012 RGO:31013 neoplasm of acetabulum RGO:31013 RGO:31014 acetabular fracture RGO:31014 RGO:31015 pubic bone nonossification RGO:31015 RGO:31016 delayed ossification of the pubic bone RGO:31016 SNOMEDCT:13277001 RGO:31017 cystic acne RGO:31017 RGO:31018 multicentric infantile fibromatosis RGO:31018 RGO:31019 familial multiple nonossifying lipoma RGO:31019 HP:0009760 ORDO:2987 RGO:31021 antecubital pterygium RGO:31021 RGO:31023 extradural cyst RGO:31023 RGO:31024 intraspinal lipoma RGO:31024 RGO:31025 bilateral sacroiliac joint abnormality RGO:31025 RGO:31026 sacroiliac joint abnormality RGO:31026 HP:0031371 SNOMEDCT:10825001 RGO:31027 rectal perforation RGO:31027 RGO:31029 sacrococcygeal mass RGO:31029 RGO:31030 intramedullary mass RGO:31030 ICD10CM:B39.5 RGO:31031 histoplasmosis duboisii RGO:31031 RGO:31032 cystic-type lymphangiomatosis RGO:31032 RGO:31033 amyloidomas RGO:31033 RGO:31036 kidney cancer metastasis RGO:31036 RGO:31038 defect in distal sternum RGO:31038 hypersegmentation of sternum RGO:31039 oversegmentation of sternum RGO:31039 RGO:31040 undersegmentation of sternum RGO:31040 congenital abnormality of the sternum RGO:31041 congenital sternal abnormality RGO:31041 RGO:31046 abnormal sternomanubrial synchondrosis RGO:31046 RGO:31047 abnormal sternoclavicular joint RGO:31047 RGO:31048 sclerosis of the sternomanubrial synchondrosis RGO:31048 RGO:31049 erosion of the sternomanubrial synchondrosis RGO:31049 RGO:31050 fusion of the sternomanubrial synchondrosis RGO:31050 RGO:31051 erosion of the sternoclavicular joint RGO:31051 RGO:31052 sclerosis of the sternoclavicular joint RGO:31052 RGO:31053 fusion of the sternoclavicular joint RGO:31053 RGO:31054 rib resection RGO:31054 RGO:31055 absent rib RGO:31055 RGO:31056 hypoplastic rib RGO:31056 RGO:31057 coarctation of thoracic aorta RGO:31057 RGO:31058 avulsed nerve root diverticulum RGO:31058 RGO:31059 congenital absence of pedicle RGO:31059 RGO:31060 congenital hypoplasia of pedicle RGO:31060 RGO:31061 congenital absence of neural arch RGO:31061 RGO:31062 congenital hypoplasia of neural arch RGO:31062 RGO:31063 arthritis with hypertrophic bony spurring RGO:31063 HP:0000960 SNOMEDCT:311897005 RGO:31064 sacral dimple RGO:31064 RGO:31065 pars interarticularis defect RGO:31065 RGO:31066 fracture with hyperextension injury RGO:31066 RADLEX:RID4669 SNOMEDCT:263070009 RGO:31067 hangman fracture RGO:31067 RGO:31068 posterior neural arch defect RGO:31068 RGO:31069 defect in C1 posterior arch RGO:31069 DOID:1036 HP:0005558 SNOMEDCT:92812005 RGO:31070 chronic leukemia RGO:31070 RGO:31071 craniometaphyseal dysplasia-like syndrome RGO:31071 RGO:31072 physiological deformity RGO:31072 RGO:31073 epiphyseal-physeal-metaphyseal injury RGO:31073 RGO:31074 juxta-articular chondroma of lateral aspect of knee RGO:31074 RGO:31075 malar flush RGO:31075 DOID:2417 SNOMEDCT:21119008 RGO:31076 pigmented nevus RGO:31076 RGO:31077 trisomy 7p RGO:31077 Richner-Hanhart syndrome ORDO:28378 RGO:31078 tyrosinemia type 2 RGO:31078 SNOMEDCT:82721003 RGO:31080 papular acrodermatitis of childhood RGO:31080 RGO:31082 lipomyeloschisis RGO:31082 RGO:31084 neurofibroma with intradural component RGO:31084 RGO:31086 ligamentum flavum thickening RGO:31086 RGO:31087 intraspinal ligament ossification RGO:31087 RGO:31089 extradural neoplasm RGO:31089 RGO:31090 intradural neoplasm RGO:31090 RGO:31091 spinal arthrosis RGO:31091 RGO:31092 tuberculous granuloma RGO:31092 SNOMEDCT:29530003 RGO:31093 fungal granuloma RGO:31093 RGO:31095 cystic osteomyelitis RGO:31095 RGO:31096 thyroid carcinoma metastasis RGO:31096 RGO:31097 cortical desmoid RGO:31097 RADLEX:RID4293 SNOMEDCT:703629008 RGO:31098 periosteal desmoid RGO:31098 RGO:31099 polycystic osteodysplasia with progressive dementia RGO:31099 RGO:31100 sickle cell disease with bone infarction RGO:31100 SNOMEDCT:178280004 RGO:31101 postnatal infection RGO:31101 SNOMEDCT:37844000 RGO:31103 chemical poisoning RGO:31103 Cornelia de Lange syndrome de Lange syndrome SNOMEDCT:40354009 RGO:31105 Brachmann-de Lange syndrome RGO:31105 DOID:0050548 RGO:31107 congenital insensitivity to pain RGO:31107 RGO:31108 psychotic state RGO:31108 RGO:31110 chromosome 2q- disorder RGO:31110 RGO:31111 chromosome 5q- disorder RGO:31111 RGO:31113 spondylometaphyseal dysplasia Algerian type RGO:31113 RGO:31114 spondylometaphyseal dysplasia Murdoch type RGO:31114 RGO:31118 juxta-articular chondroma RGO:31118 DOID:0060052 RADLEX:RID29114 SNOMEDCT:118940003 RGO:31119 neurological disorder RGO:31119 RGO:31120 pancreatic fat necrosis RGO:31120 RGO:31121 spina ventosa RGO:31121 RGO:31123 hole-in-vertebral body sign RGO:31123 HP:0100257 RGO:31126 cleft hand RGO:31126 RGO:31127 tibia hemimelia RGO:31127 RGO:31128 great toe duplication RGO:31128 RGO:31129 familial hemihypertrophy RGO:31129 HP:0001528 RGO:31130 isolated hemihypertrophy RGO:31130 RGO:31132 lethal multiple pterygium RGO:31132 RGO:31133 jackhammer operator syndrome RGO:31133 DOID:14447 HP:0000133 RADLEX:RID34626 SNOMEDCT:205681004 RGO:31135 gonadal dysgenesis RGO:31135 RGO:31136 Xq dup/partial del with X0 RGO:31136 RGO:31141 brown fat necrosis RGO:31141 RGO:31142 neuropathic state RGO:31142 RGO:31143 venous calcification RGO:31143 HP:0009776 SNOMEDCT:275348004 RGO:31144 adactyly RGO:31144 RGO:31145 monodactyly RGO:31145 HP:0009776 RGO:31147 aphalangy RGO:31147 RGO:31148 unilateral terminal transverse hand defect RGO:31148 ORDO:2730 RGO:31149 tetramelic postaxial oligodactyly RGO:31149 RGO:31150 chromosome 2q24-q31 deletion RGO:31150 RGO:31152 isolated phalangeal ivory epiphysis RGO:31152 dense epiphysis ivory epiphysis RGO:31153 sclerotic epiphysis RGO:31153 cloud-effect epiphysis fragmented epiphysis RGO:31154 irregular epiphysis RGO:31154 RGO:31163 pulmonary hamartoma syndrome RGO:31163 DOID:0060549 ORDO:1231 SNOMEDCT:408537003 RGO:31171 Barber-Say syndrome RGO:31171 SNOMEDCT:74911008 RGO:31172 congenital dyskeratosis RGO:31172 ORDO:2047 SNOMEDCT:239056006 RGO:31174 Flynn-Aird syndrome RGO:31174 RGO:31176 lethal progeroid syndrome with severe acro-osteolysis RGO:31176 Andy Gump appearance ORDO:2457 SNOMEDCT:109419009 RGO:31178 mandibuloacral dysplasia RGO:31178 SNOMEDCT:238871000 RGO:31179 metageria RGO:31179 SNOMEDCT:399947002 RGO:31180 Mulvihill-Smith syndrome RGO:31180 RGO:31181 radiation-induced progeroid syndrome RGO:31181 short stature-hyperextensibility-ocular depression-Rieger anomaly-delayed dentition syndrome ORDO:3163 RGO:31182 SHORT syndrome RGO:31182 HP:0001249 RGO:31184 mental deficiency RGO:31184 RGO:31185 an aged appearance at birth RGO:31185 RGO:31186 large helices RGO:31186 RGO:31187 eye abnormalities RGO:31187 HP:0000973 RGO:31188 lax skin RGO:31188 HP:0001388 RGO:31189 lax joints RGO:31189 RGO:31190 athetoid posturing RGO:31190 RGO:31193 neonatal premature aged appearance RGO:31193 RGO:31196 diminished facial subcutaneous fat RGO:31196 RGO:31197 low IgG level RGO:31197 RGO:31199 metaphyseal chondrodysplasia Schwachman type RGO:31199 RGO:31200 chromosome 4p16 duplication RGO:31200 RGO:31201 chromosome 22q deletion RGO:31201 RGO:31203 diffuse corticomeningeal angiomatosis RGO:31203 SNOMEDCT:211710004 SNOMEDCT:274903001 SNOMEDCT:64773009 RGO:31204 turban tumor RGO:31204 RGO:31205 Jadassohn phacomatosis RGO:31205 RGO:31206 Feuerstein-Mims syndrome RGO:31206 RGO:31207 postmeningococcal septicemia RGO:31207 RGO:31209 femur bifurcation RGO:31209 RGO:31210 tibial agenesis RGO:31210 RGO:31214 limb disuse RGO:31214 Stanescu dysostosis Stanescu osteosclerosis autosomal dominant osteosclerosis Stanescu type craniofacial dysostosis-diaphyseal hyperplasia osteosclerosis Stanescu type ORDO:1798 RGO:31217 dysostosis Stanescu type RGO:31217 HP:0000678 RGO:31220 crowded teeth RGO:31220 HP:0000691 RGO:31221 small teeth RGO:31221 HP:0002827 RGO:31222 hip dislocation RGO:31222 stubby hand RGO:31224 short hand RGO:31224 HP:0001773 SNOMEDCT:299463000 RGO:31225 short foot RGO:31225 HP:0005864 RGO:31227 isolated pseudoarthrosis RGO:31227 syndactyly type 3 RGO:31231 familial syndactyly type 3 RGO:31231 RGO:31232 duplicated great toes RGO:31232 HP:0006101 RGO:31233 finger syndactyly RGO:31233 RGO:31235 postaxial polydactyly in the hands RGO:31235 RGO:31236 preaxial polydactyly in the feet RGO:31236 RGO:31237 idiopathic vertical talus RGO:31237 HP:0001156 RGO:31240 brachydactyly syndrome RGO:31240 RGO:31241 FGFR-opathy Meunke type RGO:31241 RGO:31242 chronic vitamin A intoxication RGO:31242 RGO:31243 13-cis-retinoic acid therapy RGO:31243 RGO:31244 idiopathic cone-shaped epiphysis RGO:31244 HP:0000377 RGO:31248 malformed ears RGO:31248 HP:0000973 RGO:31249 cutaneous laxity RGO:31249 RGO:31251 distal hyperextensibility of the thumb RGO:31251 RGO:31256 head turned to one side RGO:31256 RGO:31257 adducted contracture of the hip RGO:31257 RGO:31258 truncal curvature RGO:31258 RGO:31260 congenital macrodactyly static type RGO:31260 RGO:31261 congenital macrodactyly progressive type RGO:31261 Klippel-Trénaunay syndrome DOID:2926 ICD10CM:Q87.2 SNOMEDCT:59078009 RGO:31262 Klippel-Trénaunay-Weber syndrome RGO:31262 RGO:31263 pseudomacrodactyly RGO:31263 RGO:31264 true macrodactyly RGO:31264 HP:0011304 RGO:31266 broad thumb RGO:31266 RGO:31267 large thumb RGO:31267 RGO:31268 severe shortness of the ulna and radius RGO:31268 RGO:31269 radioulnar and metacarpal synostosis RGO:31269 RGO:31270 phalangeal deformities RGO:31270 RGO:31273 cherry red spots RGO:31273 RGO:31275 prolonged use of aluminum-containing antacid RGO:31275 RGO:31276 phosphate depletion RGO:31276 RGO:31277 familial isolated tibial hemimelia RGO:31277 ORDO:93322 SNOMEDCT:79177001 RGO:31278 tibial hemimelia RGO:31278 HP:0001829 RGO:31279 foot polydactyly RGO:31279 HP:0009556 RGO:31280 absent tibia RGO:31280 RGO:31281 tibial hypoplasia RGO:31281 brachydactyly Temtamy type DOID:0110967 ORDO:93394 SNOMEDCT:715721005 RGO:31285 brachydactyly type A4 RGO:31285 RGO:31287 neurocele RGO:31287 SNOMEDCT:60660006 RGO:31288 Caldwell-Luc operation RGO:31288 SNOMEDCT:32288007 RGO:31289 serous cyst RGO:31289 RADLEX:RID3928 SNOMEDCT:235110008 SNOMEDCT:28727003 RGO:31290 odontogenic cyst RGO:31290 RGO:31291 keratocyst RGO:31291 RGO:31292 iatrogenic sinus cyst RGO:31292 RGO:31293 dental extraction RGO:31293 RGO:31294 sinus surgery RGO:31294 RGO:31295 nasal chromate salt abuse RGO:31295 RGO:31296 nasal cocaine abuse RGO:31296 RGO:31297 intraspinal meningocele RGO:31297 RGO:31298 increased intraspinal pressure RGO:31298 RGO:31299 spinal canal cyst RGO:31299 RGO:31300 intraabdominal neoplasm RGO:31300 RGO:31301 intraabdominal cyst RGO:31301 RGO:31303 vertebra plana RGO:31303 RGO:31305 normal young child RGO:31305 RGO:31306 short spine RGO:31306 HP:0003300 RGO:31307 ovoid vertebrae RGO:31307 RGO:31308 misshapen vertebrae RGO:31308 HP:0003307 RADLEX:RID4761 RGO:31309 lordosis RGO:31309 RGO:31310 cervical block vertebrae RGO:31310 HP:0004586 RGO:31311 codfish vertebrae RGO:31311 HP:0002773 HP:0008479 RGO:31312 small vertebrae RGO:31312 RGO:31313 narrow intervertebral disk spaces RGO:31313 DOID:10426 HP:0004602 ICD10CM:Q76.1 ORDO:2345 SNOMEDCT:5601008 RGO:31314 Klippel-Feil syndrome RGO:31314 RGO:31315 missing vertebra RGO:31315 RGO:31316 sacral dysplasia RGO:31316 RGO:31317 craniocervical junction abnormality RGO:31317 RGO:31318 collapsed vertebrae RGO:31318 RGO:31319 C1-C2 instability RGO:31319 RGO:31320 lack of weight bearing RGO:31320 RGO:31322 intervertebral calcification RGO:31322 RGO:31323 scalloped vertebrae RGO:31323 RGO:31324 vertebral fusions RGO:31324 RGO:31325 occipito-atlanto-axial hypermobility RGO:31325 RGO:31326 arch defect of atlas RGO:31326 HP:0004558 RGO:31327 cervical platyspondyly RGO:31327 RGO:31328 ovoid thoracic vertebrae RGO:31328 RGO:31329 ovoid lumbar vertebrae RGO:31329 RGO:31330 narrow intervertebral disks RGO:31330 RGO:31331 C1 hypoplasia RGO:31331 HP:0003320 RGO:31332 C1-C2 subluxation RGO:31332 RGO:31333 anterior vertebral wedging RGO:31333 RGO:31334 cervical spine stenosis RGO:31334 DOID:319 HP:0002196 RADLEX:RID28802 SNOMEDCT:48522003 RGO:31335 myelopathy RGO:31335 HP:0100856 RGO:31336 poorly ossified vertebrae RGO:31336 RGO:31337 coronal vertebral cleft RGO:31337 RGO:31338 fractured vertebrae RGO:31338 SNOMEDCT:81099000 RGO:31339 cervical spinal fusion RGO:31339 RGO:31340 posterior spinal fusion RGO:31340 RGO:31341 variable vertebral agenesis in lumbosacral spine RGO:31341 HP:0002144 RGO:31342 tethered cord RGO:31342 RGO:31343 local tumor extension RGO:31343 traumatic fractures RGO:31344 traumatic fracture RGO:31344 HP:0005191 ORDO:295034 RGO:31345 congenital knee dislocation RGO:31345 RGO:31346 synovial lesion RGO:31346 RGO:31347 paragangliomata RGO:31347 SNOMEDCT:715630006 RGO:31348 universal melanosis RGO:31348 RGO:31349 familial vascular malformation RGO:31349 urinary tract malformations RGO:31350 urinary tract malformation RGO:31350 RGO:31351 upper urinary tract obstruction RGO:31351 Eagle-Barrett syndrome ORDO:2970 RGO:31352 prune-belly syndrome RGO:31352 RGO:31353 bilateral subdural hygromas RGO:31353 RGO:31354 meningeal hemangioendothelioma RGO:31354 RGO:31356 chorioangioma of the placenta RGO:31356 RGO:31357 high-output heart failure RGO:31357 HP:0001040 RGO:31358 multiple pterygia RGO:31358 RGO:31359 neuronal degeneration RGO:31359 DOID:4159 HP:0008069 SNOMEDCT:372130007 RGO:31360 skin cancer RGO:31360 HP:0010743 RGO:31364 short metatarsal RGO:31364 ORDO:90058 SNOMEDCT:90584004 RGO:31366 spinal cord injury RGO:31366 RGO:31369 biliary rickets in infancy RGO:31369 RGO:31370 osteogenesis imperfecta with trauma RGO:31370 RGO:31371 absent tibial shaft RGO:31371 RGO:31372 hypoplasia of tibial shaft RGO:31372 RGO:31373 hypoplasia of fibula RGO:31373 RGO:31374 plastic bowing fracture RGO:31374 RGO:31375 idiopathic tibial bowing RGO:31375 RGO:31376 pseudo-Madelung deformity RGO:31376 RGO:31377 Madelung-like deformity RGO:31377 ORDO:1003 RGO:31378 congenital scalp defect and postaxial polydactyly RGO:31378 RGO:31379 skin aplasia RGO:31379 DOID:2733 HP:0004334 SNOMEDCT:400190005 RGO:31380 skin atrophy RGO:31380 RGO:31381 skin hypoplasia RGO:31381 RGO:31383 congenital curved nails RGO:31383 RGO:31384 hereditary ectodermal dysplasia RGO:31384 RGO:31385 chromosome 4 abnormality RGO:31385 RGO:31387 chromosome 8 abnormality RGO:31387 RGO:31388 chromosome 9 abnormality RGO:31388 RGO:31389 nail aplasia RGO:31389 HP:0001792 RGO:31390 nail hypoplasia RGO:31390 HP:0008404 ICD10CM:L60.3 SNOMEDCT:87065009 RGO:31392 nail dystrophy RGO:31392 SNOMEDCT:201114008 RGO:31393 nail deformity RGO:31393 DOID:11249 HP:0011892 SNOMEDCT:52675005 RGO:31395 vitamin K deficiency RGO:31395 RGO:31396 maternal vitamin K depletion RGO:31396 RGO:31398 bilateral radial hypoplasia RGO:31398 RGO:31399 hypoplasia and proximally placed thumbs RGO:31399 RGO:31400 minor facial dysmorphism RGO:31400 RGO:31402 multiple epiphyseal dysplasia Fairbank type RGO:31402 RGO:31403 multiple epiphyseal dysplasia Ribbing type RGO:31403 RGO:31404 subchondral dysplasia RGO:31404 RGO:31405 osteonecrosis pubis RGO:31405 RGO:31406 expansile bone neoplasm RGO:31406 RGO:31410 multifocal osteomyelitis RGO:31410 RGO:31413 subcortical osteoporosis RGO:31413 SNOMEDCT:3398004 RGO:31414 cadmium poisoning RGO:31414 RGO:31415 chronic osteomyelitis with sequestrum and involucrum RGO:31415 RGO:31416 removal of an intramedullary rod RGO:31416 RGO:31417 treated lytic bone metastasis RGO:31417 SNOMEDCT:27881006 SNOMEDCT:443092002 RGO:31419 bony callus RGO:31419 RGO:31420 treated lytic bone metastases RGO:31420 RGO:31421 treated multiple myeloma RGO:31421 RGO:31423 multiple enchondromas RGO:31423 SNOMEDCT:237311001 RGO:31425 breech delivery RGO:31425 RGO:31426 idiopathic metaphyseal spur RGO:31426 RGO:31427 Pelkan spur RGO:31427 metaphyseal horn RGO:31428 metaphyseal spur RGO:31428 fragmented metaphysis RGO:31429 metaphyseal fragmentation RGO:31429 RGO:31432 corner fracture in infants RGO:31432 RGO:31433 growth acceleration lines RGO:31433 RGO:31436 maternal estrogen therapy during pregnancy RGO:31436 RGO:31437 maternal heavy metal therapy during pregnancy RGO:31437 RGO:31438 cystic lymphangiomatosis RGO:31438 DOID:2256 SNOMEDCT:240190009 RGO:31439 osteochondrodysplasia RGO:31439 DOID:1934 SNOMEDCT:109420003 RGO:31440 dysostosis RGO:31440 RGO:31441 chronic avulsive injury of bone cortex RGO:31441 HP:0012418 ICD10CM:R09.02 SNOMEDCT:389087006 RGO:31442 hypoxemia RGO:31442 RGO:31443 chronic pulmonary disease RGO:31443 SNOMEDCT:3345002 RGO:31444 idiopathic osteoporosis RGO:31444 RGO:31447 upper limb malformation RGO:31447 RGO:31448 lower limb malformation RGO:31448 RGO:31449 pelvic deformity RGO:31449 RGO:31450 thoracic dystrophy RGO:31450 HP:0003022 RGO:31451 short ulna RGO:31451 HP:0002984 RGO:31452 short radius RGO:31452 RGO:31453 Michels syndrome-like RGO:31453 RGO:31454 distal forearm exostosis RGO:31454 RGO:31455 ulnar ray aplasia RGO:31455 HP:0003022 RGO:31456 ulnar hypoplasia RGO:31456 RGO:31457 ulnar aplasia RGO:31457 RGO:31458 bilateral symmetrical deficiency of the fifth digital rays of all four limbs RGO:31458 RGO:31459 severe limb deformity RGO:31459 RGO:31461 chromosome 4p disorder RGO:31461 ORDO:261344 RGO:31462 trisomy 1q RGO:31462 RGO:31465 increased nuchal fold RGO:31465 nuchal cyst RGO:31466 nuchal cystic hygroma RGO:31466 RGO:31467 chromosome 13p partial deletion RGO:31467 RGO:31468 trisomy 16 RGO:31468 XO/XX mosaicism RGO:31469 chromosome 45,X/46,XX mosaicism RGO:31469 RGO:31471 Bart hemoglobinopathy RGO:31471 RGO:31474 warfarin therapy in childhood RGO:31474 RGO:31475 chondral calcification RGO:31475 HP:0025477 SNOMEDCT:237898004 RGO:31476 periarticular calcification RGO:31476 RGO:31477 cheiroarthropathy RGO:31477 DOID:848 HP:0001369 RADLEX:RID3553 SNOMEDCT:3723001 RGO:31479 arthritis RGO:31479 RGO:31484 familial degenerative osteoarthropathy RGO:31484 ORDO:3310 SNOMEDCT:715530004 RGO:31487 tetrasomy 9p RGO:31487 RGO:31489 patellar dysplasia RGO:31489 RGO:31490 multipartite patella RGO:31490 ORDO:295041 ORDO:86789 RGO:31491 familial patella hypoplasia RGO:31491 HP:0010498 SNOMEDCT:79214007 RGO:31492 bipartite patella RGO:31492 DOID:9353 HP:0001374 RGO:31493 congenital hip dislocation RGO:31493 RGO:31494 flat femoral head RGO:31494 RGO:31495 fragmented femoral head RGO:31495 RGO:31498 radius hypoplasia RGO:31498 RGO:31499 segmentation abnormality of the 2nd metacarpal RGO:31499 RGO:31500 nonsyndromic brachymetacarpalia RGO:31500 RGO:31501 hypovascularity RGO:31501 RGO:31503 cane-shaped epiphyses RGO:31503 RGO:31504 central epiphyseometaphyseal fusion RGO:31504 RGO:31505 meningococcal osteomyelitis RGO:31505 RGO:31506 tetrasomy 20p RGO:31506 irregular metaphysis HP:0003025 RGO:31509 metaphyseal irregularity RGO:31509 HP:0004979 RGO:31510 metaphyseal sclerosis RGO:31510 RGO:31513 familial Wilms tumor RGO:31513 ORDO:2504 RGO:31515 metaphyseal dysplasia with maxillary hypoplasia and brachydactyly RGO:31515 RGO:31516 distal bifurcation of humerus RGO:31516 RGO:31517 partial aplasia of lower limb RGO:31517 DOID:14766 HP:0000104 RGO:31518 renal aplasia RGO:31518 RGO:31520 intra-articular chondroma RGO:31520 DOID:14107 RGO:31521 de Quervain disease RGO:31521 RGO:31522 avulsive trauma RGO:31522 RGO:31523 physiologic degenerative change RGO:31523 RGO:31524 aponeurotic-type fibromatosis RGO:31524 RGO:31525 calcification in a ligament RGO:31525 RGO:31526 calcification in a tendon RGO:31526 HP:0011467 RGO:31527 absent gallbladder RGO:31527 HP:0012210 RGO:31528 kidney malformation RGO:31528 RGO:31529 radial limb deficiency RGO:31529 RGO:31531 intravascular coagulation RGO:31531 RGO:31537 aphalangia RGO:31537 HP:0004050 ORDO:294983 SNOMEDCT:371199008 RGO:31538 acheiria RGO:31538 HP:0011301 ORDO:294986 RGO:31539 apodia RGO:31539 RGO:31540 preaxial polysyndactyly RGO:31540 RGO:31541 postaxial polysyndactyly RGO:31541 RGO:31542 crossed polydactyly type 1 RGO:31542 RGO:31543 crossed polydactyly type 2 RGO:31543 RGO:31544 postaxial polydactyly of the hand RGO:31544 ORDO:295006 RGO:31545 preaxial polydactyly of the foot RGO:31545 RGO:31546 preaxial polydactyly of the hand RGO:31546 ORDO:295008 RGO:31547 postaxial polydactyly of the foot RGO:31547 RGO:31550 leiomyomatosis of esophagus RGO:31550 HP:0000790 ICD10CM:R31 RADLEX:RID34774 SNOMEDCT:34436003 RGO:31551 hematuria RGO:31551 DOID:4586 RGO:31553 familial meningioma RGO:31553 RGO:31554 glomus jugularis tumor RGO:31554 RGO:31556 familial Leydig cell tumor RGO:31556 RGO:31557 familial ganglioneuroma RGO:31557 RGO:31558 familial neuroblastoma RGO:31558 RGO:31559 familial ganglioneuroblastoma RGO:31559 RGO:31560 familial paraganglioneuroma RGO:31560 RGO:31561 familial extra-adrenal pheochromocytoma RGO:31561 RGO:31562 noncleavage of cerebellum RGO:31562 RGO:31563 pretibial hemangioma RGO:31563 HP:0002335 RGO:31564 agenesis of cerebellar vermis RGO:31564 DOID:486 HP:0031357 SNOMEDCT:403976007 RGO:31565 glomeruloid hemangioma RGO:31565 RGO:31566 chest wall hemangioma RGO:31566 RGO:31569 carcinomatous infiltration RGO:31569 SNOMEDCT:262754009 RGO:31570 orbital trauma RGO:31570 SNOMEDCT:37058002 RGO:31571 foreign body reaction RGO:31571 RGO:31572 orbital neurofibroma RGO:31572 RGO:31573 extradural arteriovenous fistula RGO:31573 sinusitis RGO:31574 paranasal sinusitis RGO:31574 RGO:31576 severe craniosynostosis RGO:31576 RGO:31577 orbital meningocele RGO:31577 HP:0007115 SNOMEDCT:15671007 RGO:31578 orbital encephalocele RGO:31578 RGO:31579 orbital meningioma RGO:31579 RGO:31580 sphenoid ridge meningioma RGO:31580 RGO:31581 fracture with orbital emphysema RGO:31581 RGO:31582 fracture with retro-orbital hematoma RGO:31582 RGO:31583 retrobulbar abscess RGO:31583 RGO:31584 retrobulbar cellulitis RGO:31584 RGO:31585 retrobulbar myositis RGO:31585 RGO:31586 periorbital abscess RGO:31586 HP:0100539 ICD10CM:L03.213 SNOMEDCT:109245003 RGO:31587 periorbital cellulitis RGO:31587 RGO:31588 periorbital myositis RGO:31588 SNOMEDCT:253075001 SNOMEDCT:87364003 RGO:31589 sympathicoblastoma RGO:31589 RGO:31590 small optic canal RGO:31590 HP:0012777 RGO:31592 retinal neoplasm RGO:31592 RGO:31593 choroidal neoplasm RGO:31593 RGO:31594 scleral neoplasm RGO:31594 thickening of the orbital roof RGO:31599 sclerosis of the orbital roof RGO:31599 RGO:31602 inflammatory lymphadenopathy RGO:31602 ICD10CM:K09.8 RADLEX:RID3914 SNOMEDCT:129141005 RGO:31606 lymphoepithelial cyst RGO:31606 RGO:31607 salivary duct stricture RGO:31607 RGO:31608 hormonal disturbance RGO:31608 RGO:31609 idiopathic salivary gland enlargement RGO:31609 RGO:31610 lipomatous pseudohypertrophy of parotid RGO:31610 RGO:31611 cementoosseous dysplasia RGO:31611 RGO:31612 immature dentinoma RGO:31612 SNOMEDCT:302863006 SNOMEDCT:80699009 RGO:31613 cemento-ossifying fibroma RGO:31613 RGO:31614 midpalatine cyst RGO:31614 RGO:31615 aneurysm in bone RGO:31615 RGO:31616 postextraction tooth socket RGO:31616 ORDO:33108 SNOMEDCT:60192008 RGO:31617 lethal multiple pterygium syndrome RGO:31617 SNOMEDCT:23566007 RGO:31619 Listeria RGO:31619 SNOMEDCT:409822003 SNOMEDCT:41146007 RGO:31620 bacteria RGO:31620 RGO:31621 trisomy 15 RGO:31621 RGO:31622 chromosomes 15 and 17 partial duplication RGO:31622 RGO:31623 chromosome 17q- RGO:31623 RGO:31624 chromosome 18 short arm partial deletion RGO:31624 RGO:31625 chromosome 18 partial duplication RGO:31625 RGO:31626 soft-tissue tumor RGO:31626 RGO:31627 placental chorioangioma RGO:31627 DOID:2024 RGO:31628 placental choriocarcinoma RGO:31628 HP:0002390 SNOMEDCT:261482004 RGO:31630 spinal arteriovenous malformation RGO:31630 RGO:31631 ciguatera poisoning RGO:31631 RGO:31632 amastia and ureteral triplication RGO:31632 RGO:31635 amastia-athelia-ectodermal dysplasia RGO:31635 RGO:31639 congenital anorectal malformation RGO:31639 RGO:31640 congenital genital malformation RGO:31640 RGO:31641 congenital urinary tract malformation RGO:31641 RGO:31642 early osteitis pubis RGO:31642 RGO:31643 degenerative changes RGO:31643 RGO:31644 healed osteitis pubis RGO:31644 RGO:31645 pseudomarsupial bones RGO:31645 RGO:31646 idiopathic pubic fusion RGO:31646 osteonecrosis of the ischiopubic synchondrosis RADLEX:RID29082 RGO:31649 Van Neck disease RGO:31649 osteonecrosis of the ischial apophysis RADLEX:RID29076 RGO:31650 Milch disease RGO:31650 osteonecrosis of the symphysis pubis RADLEX:RID29078 RGO:31651 Pierson disease RGO:31651 osteonecrosis of the medial epicondyle of the humerus RGO:31652 Adams disease RGO:31652 osteonecrosis of the femoral condyle in adults RADLEX:RID29058 RGO:31654 Ahlback disease RGO:31654 osteonecrosis of the medial malleolus RGO:31656 Breck disease RGO:31656 osteonecrosis of the femoral head RGO:31658 Chandler disease RGO:31658 osteonecrosis of the talus RADLEX:RID29064 RGO:31659 Diaz disease RGO:31659 Freiberg disease osteonecrosis of second metatarsal head RADLEX:RID5370 RGO:31662 Freiberg infraction RGO:31662 RGO:31663 atypical laryngocele RGO:31663 SNOMEDCT:103442008 RGO:31665 Haemophilus influenzae type B RGO:31665 RGO:31666 hot air inhalation RGO:31666 RADLEX:RID3966 SNOMEDCT:302857002 SNOMEDCT:60392001 RGO:31667 angiofibroma RGO:31667 DOID:2691 RADLEX:RID4389 SNOMEDCT:66357004 RGO:31669 myoma RGO:31669 RGO:31670 congenital retention cyst RGO:31670 DOID:139 SNOMEDCT:63451008 RGO:31671 squamous cell papilloma RGO:31671 RGO:31672 mediastinal neoplasm RGO:31672 SNOMEDCT:283545005 SNOMEDCT:56768003 RGO:31673 gunshot wound RGO:31673 RGO:31674 disorder of recurrent laryngeal nerve RGO:31674 DOID:3437 SNOMEDCT:45913009 RGO:31675 laryngitis RGO:31675 RGO:31676 cerebral lesion RGO:31676 SNOMEDCT:56110009 RGO:31677 birth injury RGO:31677 SNOMEDCT:13619001 RGO:31678 thyroidectomy RGO:31678 SNOMEDCT:45685007 RGO:31679 radical neck dissection RGO:31679 increased retropharyngeal space RGO:31681 increased prevertebral space RGO:31681 RGO:31684 spinal inflammation RGO:31684 RGO:31685 prevertebral hematoma RGO:31685 RGO:31686 prevertebral edema RGO:31686 Schmincke tumor carcinoma of nasopharynx DOID:9261 ORDO:150 SNOMEDCT:449248000 RGO:31687 nasopharyngeal carcinoma RGO:31687 DOID:8557 RGO:31688 oropharyngeal carcinoma RGO:31688 RGO:31689 traumatic pharyngeal pseudodiverticulum RGO:31689 RGO:31690 spinal metastasis RGO:31690 RGO:31691 primary spinal neoplasm RGO:31691 RGO:31692 phrenic nerve trauma RGO:31692 RGO:31693 brachial plexus trauma RGO:31693 RGO:31694 cervical spine trauma RGO:31694 RGO:31695 chest wall trauma RGO:31695 RGO:31696 subphrenic mass RGO:31696 RGO:31697 cystic sarcoidosis RGO:31697 anaesthesia RADLEX:RID11006 SNOMEDCT:33653009 RGO:31698 anesthesia RGO:31698 RGO:31699 airway foreign body RGO:31699 SNOMEDCT:38013005 SNOMEDCT:86553008 RGO:31700 immunosuppression RGO:31700 SNOMEDCT:402426007 RGO:31702 rheumatoid nodulosis RGO:31702 RGO:31703 intra-articular ganglion RGO:31703 RGO:31705 achondroplasia homozygous type RGO:31705 HP:0010584 RGO:31706 pseudoepiphyses RGO:31706 RGO:31707 accessory epiphyses RGO:31707 HP:0002863 RGO:31710 myelodysplasia RGO:31710 HP:0010884 RGO:31714 acromelia RGO:31714 RGO:31715 weightlifting RGO:31715 SNOMEDCT:263019000 RGO:31716 dislocation of acromioclavicular joint RGO:31716 RGO:31717 sternoclavicular joint osteoarthritis RGO:31717 RGO:31718 acromioclavicular joint osteoarthritis RGO:31718 RGO:31719 septic arthritis of the sternoclavicular joint RGO:31719 RGO:31720 septic arthritis of the acromioclavicular joint RGO:31720 DA2A Freeman-Sheldon syndrome cranio-carpo-tarsal syndrome craniocarpotarsal dysplasia whistling face syndrome windmill-vane-hand syndrome RGO:31724 distal arthrogryposis type 2A RGO:31724 RGO:31725 birth trauma to brachial plexus RGO:31725 DOID:13137 SNOMEDCT:64383006 RGO:31726 Werdnig-Hoffmann disease RGO:31726 hypoplastic clavicle RGO:31727 clavicle hypoplasia RGO:31727 SNOMEDCT:298764003 RGO:31728 thin clavicle RGO:31728 aplasia of the clavicle aplastic clavicle clavicle aplasia clavicular aplasia RGO:31729 absent clavicle RGO:31729 RGO:31733 sclerotic clavicle RGO:31733 RGO:31734 periosteal reaction involving the clavicle RGO:31734 RGO:31735 glenohumeral joint arthritis RGO:31735 SNOMEDCT:17211005 RGO:31736 winged scapula RGO:31736 RGO:31737 traumatic pseudoarthrosis RGO:31737 SNOMEDCT:302847003 SNOMEDCT:30924005 RGO:31752 rhabdosarcoma RGO:31752 DOID:11054 HP:0009725 SNOMEDCT:399326009 RGO:31753 bladder cancer RGO:31753 SNOMEDCT:237772002 RGO:31756 adrenal atrophy RGO:31756 RGO:31757 adrenopause RGO:31757 RGO:31758 steroid-producing nonendocrine neoplasm RGO:31758 HP:0030357 SNOMEDCT:254633006 RGO:31759 oat cell carcinoma of lung RGO:31759 RGO:31760 experimental hyperoxia RGO:31760 SNOMEDCT:372877000 SNOMEDCT:84812008 RGO:31761 heparin RGO:31761 RGO:31762 excessive steroids RGO:31762 RGO:31764 poorly controlled diabetes RGO:31764 RGO:31765 pituitary abnormality RGO:31765 RGO:31766 basophilic pituitary adenoma RGO:31766 RGO:31767 phosphorus deficiency RGO:31767 SNOMEDCT:238117007 RGO:31768 calcium deficiency RGO:31768 RGO:31769 GM1 galactisidosis RGO:31769 RGO:31770 myotonica congenita RGO:31770 RGO:31771 breast cancer metastases RGO:31771 ICD10CM:M89.0 SNOMEDCT:2103002 RGO:31772 shoulder-hand syndrome RGO:31772 SNOMEDCT:211236007 RGO:31773 scalenus anticus syndrome RGO:31773 RADLEX:RID5364 SNOMEDCT:425852005 RGO:31774 fracture malunion RGO:31774 RGO:31775 fracture infection RGO:31775 RGO:31776 diabetic osteopathy RGO:31776 RGO:31777 bone marrow edema syndrome RGO:31777 SNOMEDCT:240159007 RGO:31778 transient osteoporosis of hip RGO:31778 RGO:31779 idiopathicdemineralization RGO:31779 RADLEX:RID5054 SNOMEDCT:286792001 SNOMEDCT:66277009 RGO:31780 denervation RGO:31780 RGO:31781 tendon transection RGO:31781 DOID:3223 ORDO:83452 SNOMEDCT:128200000 RGO:31783 complex regional pain syndrome RGO:31783 causalgia ORDO:99994 RGO:31784 complex regional pain syndrome type 2 RGO:31784 RGO:31786 multiple primary bone neoplasms RGO:31786 RGO:31787 traumatic osteochondral injury RGO:31787 RGO:31788 small-particle disease RGO:31788 RGO:31789 multicentric bone sarcoma RGO:31789 RGO:31792 Thorotrast injection RGO:31792 RGO:31793 physiologic osteosclerosis of the newborn RGO:31793 SNOMEDCT:73767002 RGO:31794 myofibromatosis RGO:31794 SNOMEDCT:7643002 RGO:31796 calcified hematoma RGO:31796 ORDO:97337 RADLEX:RID5185 RGO:31799 Sinding-Larsen-Johansson disease RGO:31799 RGO:31800 fragmented inferior tip of the patella RGO:31800 RGO:31802 maturation delay RGO:31802 RGO:31803 advanced scurvy RGO:31803 RGO:31804 widespread predominantly medullary osteosclerosis RGO:31804 RGO:31805 widespread predominantly cortical osteosclerosis RGO:31805 RGO:31806 widespread osteosclerosis of medullary and cortical bone RGO:31806 RGO:31808 metaphyseal chondrodysplasia anadysplastic type RGO:31808 HP:0011423 ICD10CM:E87.8 SNOMEDCT:74450001 RGO:31809 hyperchloremia RGO:31809 ICD10CM:E58 SNOMEDCT:190656001 RGO:31810 dietary calcium deficiency RGO:31810 RGO:31811 vitamin D-deficient rickets RGO:31811 RGO:31812 lack of sunshine RGO:31812 RGO:31813 dietary vitamin D deficiency RGO:31813 DOID:10609 SNOMEDCT:68295002 RGO:31814 vitamin D-dependent rickets RGO:31814 RGO:31815 severe myopathy RGO:31815 RGO:31816 hypophosphatemic familial rickets RGO:31816 RGO:31817 absent proximal femur RGO:31817 RGO:31818 hypoplastic proximal femur RGO:31818 RGO:31819 deformed proximal femur RGO:31819 HP:0001374 RGO:31820 congenital dislocation of the hip RGO:31820 RGO:31821 malignant bone tumor RGO:31821 ORDO:56305 RGO:31822 atelosteogenesis type 3 RGO:31822 fibular hypoplasia HP:0003038 RGO:31823 hypoplastic fibula RGO:31823 RGO:31824 absent fibula RGO:31824 HP:0003038 RGO:31825 short fibula RGO:31825 HP:0002667 RADLEX:RID4553 SNOMEDCT:302849000 RGO:31827 Wilms tumor RGO:31827 HP:0008643 RGO:31828 nephroblastomatosis RGO:31828 RGO:31829 nephrogenic rests RGO:31829 RGO:31831 cutaneous carcinoma RGO:31831 RGO:31834 soft-tissue sarcoma RGO:31834 RGO:31835 bone tumor with pathologic fracture RGO:31835 HP:0010785 RGO:31836 gonadal neoplasm RGO:31836 RADLEX:RID46039 SNOMEDCT:205465004 RGO:31839 chondrodysplasia RGO:31839 RGO:31840 metaphyseal injury RGO:31840 RGO:31841 expansile benign bone neoplasm RGO:31841 Oppenheim disease SNOMEDCT:63135006 RGO:31845 amyotonia congenita RGO:31845 SNOMEDCT:73297009 RGO:31846 progressive muscular dystrophy RGO:31846 RGO:31847 paralytic disorder RGO:31847 RGO:31848 congenital spinal cord malformation RGO:31848 DOID:3615 SNOMEDCT:24045002 RGO:31849 infiltrating angiolipoma RGO:31849 RGO:31850 chronic lymphatic obstruction RGO:31850 RGO:31852 congenital hypoplasia of lymphatics RGO:31852 lymph nodes RADLEX:RID13296 SNOMEDCT:181756000 SNOMEDCT:59441001 RGO:31853 lymph node RGO:31853 SNOMEDCT:30085007 RGO:31854 Morton neuroma RGO:31854 RGO:31855 nodular synovitis RGO:31855 RGO:31856 periosteal ganglion RGO:31856 RGO:31859 clavicle dysplasia RGO:31859 RGO:31864 rapid deossification RGO:31864 RGO:31867 altered calcium concentration RGO:31867 RGO:31868 altered phosphorus concentration RGO:31868 RGO:31869 neonatal subcutaneous fat necrosis RGO:31869 RGO:31870 pseudosclerema RGO:31870 RGO:31871 immobilization osteoporosis RGO:31871 RGO:31872 healing abscess RGO:31872 RGO:31873 pyogenic fibrositis RGO:31873 RGO:31874 pyogenic myositis RGO:31874 RADLEX:RID28842 SNOMEDCT:129326001 SNOMEDCT:385218009 SNOMEDCT:59108006 RGO:31875 injection RGO:31875 RGO:31876 fracture in neuromuscular disorder RGO:31876 DOID:495 SNOMEDCT:134302009 SNOMEDCT:72079004 RGO:31877 sclerosing hemangioma RGO:31877 SNOMEDCT:314994000 RGO:31878 metastatic prostate cancer RGO:31878 DOID:10952 HP:0000123 ICD10CM:N08 SNOMEDCT:52845002 RGO:31881 nephritis RGO:31881 RADLEX:RID39479 SNOMEDCT:405538007 SNOMEDCT:450423003 RGO:31882 spontaneous hemorrhage RGO:31882 RGO:31883 chronic pulmonary infection RGO:31883 RGO:31884 fungal lung infection RGO:31884 progressive pseudorheumatoid dysplasia pseudorheumatoid dysplasia RGO:31887 progressive pseudorheumatoid chondrodysplasia RGO:31887 RGO:31893 central pulmonary artery coarctation RGO:31893 RGO:31894 contralateral pulmonary embolism RGO:31894 RGO:31895 congenitally absent contralateral pulmonary artery RGO:31895 RGO:31896 hypoplastic contralateral pulmonary artery RGO:31896 RGO:31897 large unilateral pleural effusion RGO:31897 RGO:31898 unilateral pulmonary fibrosis RGO:31898 ORDO:99130 RGO:31899 partial absence of pericardium RGO:31899 RGO:31900 giant pulmonary cyst RGO:31900 RGO:31901 giant bulla RGO:31901 RGO:31902 occluded bronchus RGO:31902 RGO:31906 cortical bone desmoid RGO:31906 RGO:31911 limb hypoperfusion RGO:31911 RGO:31912 flared ilia RGO:31912 RGO:31914 trefoil-shaped pelvis RGO:31914 RGO:31915 delayed pubic ossification RGO:31915 HP:0003375 RGO:31917 small sacrosciatic notches RGO:31917 RGO:31918 squared ilia RGO:31918 RGO:31919 achondrogenesis type 1 RGO:31919 ORDO:93296 RGO:31920 achondrogenesis type 2 RGO:31920 RGO:31924 flat acetabula RGO:31924 RGO:31926 short sacroiliac notches RGO:31926 HP:0003275 RGO:31928 narrow pelvis RGO:31928 HP:0002866 RGO:31929 hypoplastic iliac wings RGO:31929 RGO:31930 trapezoid ilium RGO:31930 RGO:31931 abnormal acetabula RGO:31931 RGO:31932 squared iliac wings RGO:31932 HP:0008829 RGO:31935 delayed femoral head ossification RGO:31935 HP:0010305 RGO:31936 absent sacrum RGO:31936 RGO:31937 hypoplasia of sacrum RGO:31937 RGO:31938 short iliac wings RGO:31938 RGO:31939 flat acetabular angles RGO:31939 HP:0003375 RGO:31940 narrow sciatic notches RGO:31940 HP:0003278 RGO:31941 square pelvis RGO:31941 RGO:31942 increased iliac angle RGO:31942 RGO:31943 underdeveloped pubic rami RGO:31943 RGO:31945 primary soft-tissue neoplasm RGO:31945 RGO:31946 avulsion fracture of anterior superior iliac spine RGO:31946 RGO:31947 avulsion fracture of anterior inferior iliac spine RGO:31947 RGO:31948 multiple bruises RGO:31948 RGO:31949 healed lacerations RGO:31949 RGO:31950 burns RGO:31950 SNOMEDCT:38146002 RGO:31951 underdevelopment RGO:31951 RGO:31952 poor hygiene RGO:31952 SNOMEDCT:33737001 RGO:31953 rib fracture RGO:31953 Hornstein-Birt-Hogg-Dubé syndrome Hornstein-Knickenberg syndrome fibrofolliculomas with trichodiscomas and acrochordons DOID:0050676 ORDO:122 SNOMEDCT:110985001 RGO:31954 Birt-Hogg-Dubé syndrome RGO:31954 RGO:31955 hair follicle hamartoma RGO:31955 DOID:2513 HP:0002671 SNOMEDCT:1338007 RGO:31958 basal cell carcinoma RGO:31958 DOID:6808 SNOMEDCT:254705003 RGO:31961 basaloid follicular hamartoma RGO:31961 HP:0008696 RGO:31962 renal hamartoma RGO:31962 SNOMEDCT:254044004 RGO:31964 hereditary multiple exostosis RGO:31964 osteoporosis circumscripta DOID:5408 RGO:31965 Paget disease of bone RGO:31965 DOID:3347 HP:0002669 SNOMEDCT:21708004 RGO:31966 osteogenic sarcoma RGO:31966 SNOMEDCT:418040002 RGO:31967 littoral cell angioma RGO:31967 SIADH DOID:3401 ICD10CM:E22.2 SNOMEDCT:55004003 RGO:31968 syndrome of inappropriate secretion of antidiuretic hormone RGO:31968 RGO:31970 sinonasal neuroendocrine carcinoma RGO:31970 DOID:686 SNOMEDCT:109841003 RGO:31971 liver carcinoma RGO:31971 RGO:31973 osteochondral injury RGO:31973 RGO:31974 epiphyseal lytic lesion RGO:31974 RGO:31975 apophyseal lytic lesion RGO:31975 RGO:31976 sesamoid lytic lesion RGO:31976 RGO:31980 subacute bacterial osteomyelitis RGO:31980 RGO:31981 chronic bacterial osteomyelitis RGO:31981 RGO:31982 reactive periostitis RGO:31982 RGO:31983 diabetic ulcer RGO:31983 SNOMEDCT:118619002 RGO:31984 deep abscess RGO:31984 hair-on-end periosteal reaction RGO:31987 parallel spiculated periosteal reaction RGO:31987 sunburst periosteal reaction RGO:31988 divergent spiculated periosteal reaction RGO:31988 RGO:31992 neuroblastoma metastasis RGO:31992 RGO:31993 prostate carcinoma metastasis RGO:31993 RGO:31994 Ewing sarcoma metastasis RGO:31994 RGO:31995 physiological periostitis of the newborn RGO:31995 HP:0010885 RGO:31996 multiple bone infarction RGO:31996 RGO:31999 osteomalacia with fractures RGO:31999 RADLEX:RID49608 RGO:32000 vertebral fracture RGO:32000 RGO:32001 metaphyseal infraction RGO:32001 RADLEX:RID4653 SNOMEDCT:23482006 RGO:32002 avulsion fracture RGO:32002 HP:0003908 RGO:32003 bucket handle fracture RGO:32003 RGO:32004 corner fracture RGO:32004 ODDD syndrome oculodentodigital dysplasia RGO:32018 Meyer-Schwickerath syndrome RGO:32018 RGO:32019 mandibular nerve neurofibroma RGO:32019 RGO:32020 postextraction defect RGO:32020 RGO:32021 avulsion fracture defect RGO:32021 RGO:32022 choroidal metastasis RGO:32022 RGO:32023 primary melanoma RGO:32023 DOID:2415 RADLEX:RID4374 SNOMEDCT:26325004 RGO:32024 melanocytoma RGO:32024 RGO:32025 bacterial sinus infection RGO:32025 RGO:32026 traumatic carotid-cavernous fistula RGO:32026 RGO:32027 cystic chondrosarcoma RGO:32027 RGO:32028 lacrimal gland inflammation RGO:32028 RGO:32029 lacrimal gland sarcoidosis RGO:32029 RGO:32030 benign mixed tumor of lacrimal gland RGO:32030 DOID:4870 SNOMEDCT:254987003 RGO:32031 adenoid cystic carcinoma of lacrimal gland RGO:32031 RGO:32032 lacrimal gland lymphoma RGO:32032 RGO:32034 optic nerve lesion RGO:32034 RGO:32035 optic nerve sheath lesion RGO:32035 RGO:32036 facial nerve vascular hamartoma RGO:32036 RGO:32037 cranial nerve VIII schwannoma RGO:32037 SNOMEDCT:80595007 RGO:32038 glomus tympanicum RGO:32038 RGO:32039 parotid lymphoepithelial cysts RGO:32039 SNOMEDCT:240526004 RGO:32040 epidemic parotitis RGO:32040 SNOMEDCT:73381000119100 RGO:32042 second branchial cleft cyst RGO:32042 RGO:32043 glomus caroticum RGO:32043 RGO:32044 jugular thrombophlebitis RGO:32044 RGO:32045 infectious lymphadenopathy RGO:32045 ICD10CM:M85.4 ORDO:83468 RADLEX:RID3945 SNOMEDCT:112643007 SNOMEDCT:203467005 RGO:32047 solitary bone cyst RGO:32047 RGO:32048 immature ossifying fibroma RGO:32048 RGO:32049 systemic lymphoma RGO:32049 RGO:32050 primary lymphoma RGO:32050 RGO:32051 parotid lymphoepithelial cyst RGO:32051 RGO:32052 metastasis to salivary gland RGO:32052 SNOMEDCT:254651007 RGO:32054 cutaneous squamous cell carcinoma RGO:32054 SNOMEDCT:38549000 RGO:32055 undifferentiated carcinoma RGO:32055 RGO:32056 wide flared ilia RGO:32056 HP:0003375 RGO:32057 small sacrosciatic notch RGO:32057 RGO:32058 broad pubis RGO:32058 HP:0100865 RGO:32059 broad ischia RGO:32059 HP:0003180 RGO:32060 flat acetabular roofs RGO:32060 RGO:32061 unossified pubic bones RGO:32061 RGO:32062 vertical ischia RGO:32062 RGO:32063 short ilia RGO:32063 RGO:32064 small sacroiliac incisura RGO:32064 HP:0004590 RGO:32065 small sacrum RGO:32065 RGO:32066 small iliac height RGO:32066 RGO:32067 wide pelvic cavity RGO:32067 RGO:32068 vertical ilia RGO:32068 HP:0009780 RGO:32069 iliac horns RGO:32069 RGO:32070 small iliac index RGO:32070 HP:0002869 RGO:32071 flared iliac wings RGO:32071 RGO:32072 steep acetabular roofs RGO:32072 RGO:32073 narrow pelvic inlet RGO:32073 RGO:32074 tapered ischia RGO:32074 RGO:32075 minor salivary gland carcinoma RGO:32075 RGO:32076 epidural tumor RGO:32076 RGO:32077 extramedullary mass RGO:32077 RGO:32078 severe spondylosis RGO:32078 RGO:32079 intramedullary tumor RGO:32079 RGO:32080 extramedullary tumor RGO:32080 RGO:32081 posterior fossa mass RGO:32081 DOID:327 HP:0003396 ORDO:3280 SNOMEDCT:111496009 RGO:32082 syringomyelia RGO:32082 HP:0100565 ICD10CM:Q06.4 RADLEX:RID34643 SNOMEDCT:11197005 RGO:32083 hydromyelia RGO:32083 ICD10CM:G93.81 RGO:32084 mesial temporal sclerosis RGO:32084 RGO:32085 unilateral obstruction of foramen of Monro RGO:32085 RGO:32086 venous cerebral infarction RGO:32086 DOID:0060068 SNOMEDCT:57181007 RGO:32090 marantic endocarditis RGO:32090 RGO:32091 cardiac mural thrombus RGO:32091 SNOMEDCT:17289003 SNOMEDCT:212372004 RGO:32092 fat embolus RGO:32092 RGO:32093 carotid dissection RGO:32093 RADLEX:RID10365 RGO:32094 catheter angiography RGO:32094 RGO:32095 infectious endocarditis RGO:32095 RGO:32096 inferior vena cava thrombus RGO:32096 RGO:32097 ulcerated carotid plaque platelet embolus RGO:32097 RGO:32099 atypical branchial cleft cyst RGO:32099 RGO:32100 cystic salivary gland neoplasm RGO:32100 RGO:32101 pyogenic adenitis RGO:32101 SNOMEDCT:95205002 RGO:32102 pharyngeal perforation RGO:32102 RGO:32103 large intracranial arteriovenous malformation RGO:32103 RGO:32104 cervical spine injury RGO:32104 RGO:32105 cervical spine fracture RGO:32105 RGO:32106 enlarged lymphoid tissue RGO:32106 ICD10CM:Q31.1 ORDO:141121 SNOMEDCT:204552001 RGO:32108 congenital subglottic stenosis RGO:32108 RGO:32110 ectopic intratracheal thyroid tissue RGO:32110 RGO:32111 ectopic goiter RGO:32111 RGO:32112 ectopic intratracheal thymus tissue RGO:32112 RGO:32113 localized retropharyngeal abscess RGO:32113 RGO:32114 subglottic hemangioma RGO:32114 RGO:32115 inflammatory histiocytoma RGO:32115 RGO:32117 polypoid hemangioendothelioma RGO:32117 RGO:32118 aspirated tracheal foreign body RGO:32118 RGO:32119 impacted food RGO:32119 SNOMEDCT:311721007 RGO:32120 lye RGO:32120 RGO:32121 acid aspiration RGO:32121 floppy trachea RGO:32122 normal expiratory collapse RGO:32122 RGO:32123 anterior tracheal indentation RGO:32123 RGO:32125 posttracheostomy fibrosis RGO:32125 RGO:32126 innominate artery compression RGO:32126 RGO:32127 aryepiglottic fold cyst RGO:32127 RGO:32128 micrognathia with glossoptosis RGO:32128 HP:0000347 RGO:32129 isolated micrognathia RGO:32129 RGO:32130 angioneurotic laryngeal edema RGO:32130 RGO:32131 inhalation of noxious gases RGO:32131 RGO:32132 traumatic laryngeal edema RGO:32132 SNOMEDCT:82966003 RGO:32134 hereditary angioneurotic edema RGO:32134 RGO:32135 anaphylactic angioneurotic edema RGO:32135 RGO:32136 allergic angioneurotic edema RGO:32136 RGO:32137 retropharyngeal hemorrhage RGO:32137 RGO:32138 neck surgery RGO:32138 RGO:32140 traumatic tracheal stricture RGO:32140 RGO:32141 prolonged intubation RGO:32141 RGO:32142 postoperative tracheal stricture RGO:32142 RGO:32143 inflammatory tracheal stricture RGO:32143 SNOMEDCT:11296007 RGO:32144 tracheal stricture RGO:32144 RGO:32145 hamartochondroma RGO:32145 RGO:32147 tracheal web RGO:32147 SNOMEDCT:86423004 RGO:32148 laryngeal polyp RGO:32148 HP:0100640 RGO:32149 laryngeal cyst RGO:32149 RGO:32150 laryngeal papilloma RGO:32150 RGO:32152 root sleeve avulsion RGO:32152 RGO:32153 C1-C2 subluxation in rheumatoid arthritis RGO:32153 RADLEX:RID10008 SNOMEDCT:2048000 SNOMEDCT:276957006 RGO:32156 lingual tonsil RGO:32156 RGO:32157 atypical ranula RGO:32157 DOID:248 RGO:32158 tracheal tumor RGO:32158 RGO:32159 epiglottic enlargement RGO:32159 HP:0008749 ICD10CM:Q31.2 SNOMEDCT:253736003 RGO:32160 laryngeal hypoplasia RGO:32160 HP:0005950 ORDO:2374 SNOMEDCT:297159008 RGO:32161 laryngeal web RGO:32161 HP:0001605 SNOMEDCT:302912005 RGO:32163 vocal cord paralysis RGO:32163 RGO:32164 recurrent laryngeal nerve invasion RGO:32164 RGO:32165 congenital vocal cord paralysis RGO:32165 SNOMEDCT:448665005 RGO:32166 carcinoma of hypopharynx RGO:32166 RGO:32168 intramedullary chondrosarcoma with soft-tissue extension RGO:32168 RGO:32169 intramedullary osteosarcoma with soft-tissue extension RGO:32169 RGO:32170 carcinoma arising from chronic osteomyelitis RGO:32170 RGO:32171 carcinoma arising from tropical ulcer RGO:32171 RGO:32172 cyst-like dactylitis RGO:32172 RGO:32173 synovial herniation pit of femoral neck RGO:32173 RGO:32174 solitary lytic epiphyseal lesion RGO:32174 RGO:32175 solitary lytic epiphyseal-metaphyseal lesion RGO:32175 RGO:32176 arthritic subchondral cyst RGO:32176 RGO:32177 traumatic subchondral cyst RGO:32177 RGO:32178 hepatocellular carcinoma metastasis RGO:32178 RGO:32179 thyroid cancer metastasis RGO:32179 RGO:32180 renal cell carcinoma metastasis RGO:32180 RGO:32181 traumatic callus formation RGO:32181 RGO:32182 physiologic periostitis of the newborn RGO:32182 RGO:32183 retinoblastoma metastasis RGO:32183 RGO:32184 embryonal rhabdomyosarcoma metastasis RGO:32184 RGO:32185 cystic pleomorphic adenoma RGO:32185 RGO:32186 primary salivary gland cyst RGO:32186 RGO:32187 necrotic lymph node metastasis RGO:32187 RGO:32188 parotid enlargement RGO:32188 RGO:32189 acute parotitis RGO:32189 RGO:32190 recurrent pyogenic parotitis RGO:32190 RADLEX:RID3659 SNOMEDCT:41569004 RGO:32191 sialodochitis RGO:32191 HP:0005523 RADLEX:RID3839 SNOMEDCT:277466009 SNOMEDCT:414629003 RGO:32192 lymphoproliferative disorder RGO:32192 RGO:32193 salivary duct stone RGO:32193 RGO:32194 chronic punctate sialadenitis RGO:32194 DOID:13212 RGO:32196 metastatic skin carcinoma RGO:32196 RGO:32197 papillary adenocystoma lymphomatosum RGO:32197 RGO:32198 cystadenolymphoma RGO:32198 salivary gland oncocytoma DOID:5389 SNOMEDCT:89439007 RGO:32199 oxyphilic adenoma RGO:32199 HP:0000677 SNOMEDCT:64969001 RGO:32201 partial anodontia RGO:32201 RGO:32204 wide tooth spacing RGO:32204 HP:0000698 SNOMEDCT:29553002 RGO:32205 conical teeth RGO:32205 RGO:32206 dental fusion RGO:32206 RGO:32207 dental enamel dysplasia RGO:32207 HP:0000675 RGO:32208 prominent upper incisors RGO:32208 RGO:32209 dental maleruption RGO:32209 RGO:32210 dental dysplasia RGO:32210 HP:0006349 RGO:32211 missing teeth RGO:32211 HP:0040079 RGO:32213 irregular teeth RGO:32213 RGO:32215 adjacent soft tissue inflammation RGO:32215 RGO:32216 neurogenic fracture RGO:32216 DOID:5859 SNOMEDCT:26211003 RGO:32217 periosteal chondrosarcoma RGO:32217 DOID:3151 SNOMEDCT:254651007 RGO:32218 squamous cell carcinoma of skin RGO:32218 RGO:32219 malignant tropical ulcer RGO:32219 SNOMEDCT:3797007 RGO:32220 periodontal cyst RGO:32220 RGO:32221 periapical dental cyst RGO:32221 RGO:32222 nasopalatine cyst RGO:32222 SNOMEDCT:81196009 RGO:32223 amputation neuroma RGO:32223 RGO:32224 focal osteoporotic bone marrow defect of the jaw RGO:32224 RGO:32225 osteomyelitis of skull base RGO:32225 SNOMEDCT:405822008 SNOMEDCT:707358000 RGO:32226 squamous cell carcinoma of larynx RGO:32226 RGO:32227 acute trauma to larynx RGO:32227 SNOMEDCT:77892009 RGO:32228 pulmonary vein thrombosis RGO:32228 SNOMEDCT:7377003 RGO:32229 sclerosing mediastinitis RGO:32229 ICD10CM:T78.2 SNOMEDCT:39579001 RGO:32230 anaphylactic reaction RGO:32230 Mendelson syndrome RGO:32231 aspiration of gastric contents RGO:32231 RGO:32234 aspiration of hydrocarbons RGO:32234 RGO:32235 aspiration of hypertonic contrast material RGO:32235 RGO:32236 beta-adrenergic drug RGO:32236 SNOMEDCT:68945006 RGO:32237 interleukin-2 RGO:32237 SNOMEDCT:36925002 RGO:32239 bronchial obstruction RGO:32239 RGO:32240 pulmonary vein obstruction RGO:32240 RGO:32241 unilateral veno-occlusive disease RGO:32241 BOOP COP bronchiolitis obliterans organizing pneumonia ORDO:1302 RGO:32242 cryptogenic organizing pneumonia RGO:32242 RGO:32246 mucus plugs RGO:32246 SNOMEDCT:196109007 RGO:32247 multiple lung abscesses RGO:32247 RGO:32248 neonatal retained fluid syndrome RGO:32248 SNOMEDCT:355001 RGO:32250 hemorrhagic shock RGO:32250 HP:0030149 ICD10CM:R57.0 ORDO:97292 SNOMEDCT:89138009 RGO:32251 cardiogenic shock RGO:32251 HP:0100845 SNOMEDCT:39579001 RGO:32252 anaphylactic shock RGO:32252 RGO:32253 multi-system organ failure RGO:32253 ICD10CM:B01.2 SNOMEDCT:195911009 RGO:32254 varicella pneumonia RGO:32254 SNOMEDCT:79877004 RGO:32255 bronchial stenosis RGO:32255 RGO:32256 healed tuberculosis RGO:32256 RGO:32257 hypoplastic pulmonary artery RGO:32257 HP:0002089 RGO:32258 hypoplastic lung RGO:32258 RGO:32259 ball-valve obstruction RGO:32259 RGO:32260 partial lung resection RGO:32260 RGO:32264 disuse RGO:32264 RGO:32265 local hyperemia RGO:32265 RGO:32266 postmastoidectomy meningoencephalocele RGO:32266 RGO:32267 postmastoidectomy meningocele RGO:32267 RGO:32268 epidural mastoid pneumatocele RGO:32268 RGO:32269 epidural mastoid cyst RGO:32269 RGO:32270 carcinoma of mastoid RGO:32270 DOID:4893 RGO:32271 carcinoma of middle ear RGO:32271 RGO:32272 erosion of tympanic portion of petrous bone RGO:32272 RGO:32273 erosion of middle ear RGO:32273 RGO:32274 erosion of mastoid RGO:32274 RGO:32275 parotid tumor RGO:32275 RGO:32276 traumatic facial nerve injury RGO:32276 RGO:32277 surgical facial nerve injury RGO:32277 RGO:32279 multiple osteomas RGO:32279 RGO:32280 tori RGO:32280 HP:0030431 RGO:32281 osteochondromas RGO:32281 SNOMEDCT:26888009 RGO:32282 odontogenic carcinoma RGO:32282 RGO:32284 odontogenic fibromyxoma RGO:32284 SNOMEDCT:26888009 RGO:32285 primary intraosseous carcinoma RGO:32285 DOID:4015 RADLEX:RID4260 SNOMEDCT:65692009 RGO:32286 spindle cell carcinoma RGO:32286 RGO:32287 hemangioendothelioma/angiosarcoma RGO:32287 RGO:32288 chronic osteitis RGO:32288 SNOMEDCT:109603007 RGO:32289 chronic alveolar abscess RGO:32289 RGO:32291 isoniazid cyst RGO:32291 RGO:32292 cavitating pneumonia RGO:32292 DOID:1082 ICD10CM:B74.8 ORDO:166291 SNOMEDCT:73328005 RGO:32293 dirofilariasis RGO:32293 RGO:32294 loculated pneumothorax RGO:32294 RGO:32295 chylomediastinum RGO:32295 RGO:32296 thoracic duct obstruction RGO:32296 RGO:32298 dilated superior vena cava RGO:32298 RGO:32303 arterial tear RGO:32303 RGO:32304 aortic transection RGO:32304 RGO:32305 malpositioned vascular catheter with vessel injury RGO:32305 RGO:32306 venous tear RGO:32306 RGO:32307 chronic pulmonary inflammation RGO:32307 RGO:32308 primary hemolytic anemia RGO:32308 RGO:32310 bone marrow injury RGO:32310 RGO:32311 benzene intoxication RGO:32311 DOID:10323 ICD10CM:J66.0 SNOMEDCT:85761009 RGO:32314 byssinosis RGO:32314 RGO:32315 cotton dust RGO:32315 RGO:32316 sugar cane dust RGO:32316 RGO:32317 auto-worker lung RGO:32317 RGO:32318 machine operator lung RGO:32318 SNOMEDCT:255771001 RGO:32319 isocyanate RGO:32319 ORDO:99908 RGO:32320 pigeon-breeder lung RGO:32320 RGO:32321 bird-fancier lung RGO:32321 RGO:32322 budgerigar lung RGO:32322 RGO:32323 ostrich feather lung RGO:32323 DOID:11289 SNOMEDCT:48347002 RGO:32324 humidifier lung RGO:32324 RGO:32325 air-conditioner lung RGO:32325 DOID:840 ICD10CM:J67.3 SNOMEDCT:13394002 RGO:32327 suberosis RGO:32327 RGO:32328 cork dust RGO:32328 RGO:32329 thesaurosis RGO:32329 SNOMEDCT:67366006 RGO:32330 hair spray RGO:32330 RGO:32331 allergic granulomatosis RGO:32331 DOID:12841 ICD10CM:B76.0 SNOMEDCT:63479002 RGO:32332 ancylostomiasis RGO:32332 RGO:32333 visceral larval migrans RGO:32333 SNOMEDCT:190055003 SNOMEDCT:37810007 RGO:32334 eosinophilic leukemia RGO:32334 RGO:32335 vagus nerve schwannoma RGO:32335 RGO:32336 dilated left superior intercostal vein RGO:32336 RGO:32337 pulmonary artery angiosarcoma RGO:32337 RGO:32339 aberrant left pulmonary artery RGO:32339 RGO:32340 squamous cell lung cancer RGO:32340 RGO:32341 large cell lung cancer RGO:32341 DOID:3910 HP:0030078 RGO:32342 lung adenocarcinoma RGO:32342 RADLEX:RID34301 RADLEX:RID3874 RADLEX:RID38780 RADLEX:RID39055 SNOMEDCT:52988006 RGO:32343 lesion RGO:32343 RGO:32344 postoperative fluid collection RGO:32344 RGO:32345 brachiocephalic artery tortuosity RGO:32345 SNOMEDCT:53320004 RGO:32347 aorticopulmonary paraganglioma RGO:32347 DOID:13186 SNOMEDCT:70667005 RGO:32348 megaesophagus RGO:32348 RGO:32353 unilateral aspiration RGO:32353 DOID:3027 SNOMEDCT:4590003 RGO:32354 metastatic adenocarcinoma RGO:32354 ICD10CM:I77.810 RGO:32355 thoracic aortic ectasia RGO:32355 fungal lung disease mycotic pneumonia SNOMEDCT:233613009 RGO:32356 fungal pneumonia RGO:32356 SNOMEDCT:300287006 RGO:32357 esophageal mass RGO:32357 DOID:117 RGO:32358 cardiac tumor RGO:32358 RGO:32359 lung granuloma RGO:32359 RGO:32360 histoplasmoma RGO:32360 RGO:32361 osteoarthritic spurring RGO:32361 RGO:32362 discogenic disease RGO:32362 RGO:32364 paraspinal hematoma RGO:32364 RGO:32366 bronchial kinking RGO:32366 RGO:32367 mucosal flap in bronchus RGO:32367 RGO:32368 enlarged fold in bronchus RGO:32368 RGO:32369 segmental bronchial atresia RGO:32369 RGO:32370 extrinsic pressure on bronchus RGO:32370 RGO:32371 idiopathic congenital lobar emphysema RGO:32371 RGO:32372 ruptured thoracic duct aneurysm RGO:32372 RGO:32373 superior vena cava thromboembolism RGO:32373 RGO:32374 left subclavian vein thromboembolism RGO:32374 RGO:32375 left brachiocephalic vein thromboembolism RGO:32375 RGO:32376 thoracic duct neoplasm RGO:32376 DOID:0060564 RGO:32377 spinal disease RGO:32377 RGO:32378 idiopathic chylothorax RGO:32378 RGO:32379 thoracic duct fistula RGO:32379 RGO:32380 organized pleural effusion RGO:32380 RGO:32381 prior pleuritis RGO:32381 RGO:32382 prior catheter drainage RGO:32382 RGO:32383 advanced pulmonary fibrosis RGO:32383 RGO:32384 advanced mediastinal fibrosis RGO:32384 RGO:32385 osteomyelitis of rib RGO:32385 RGO:32386 metastasis to rib RGO:32386 RGO:32387 prior chylothorax RGO:32387 SNOMEDCT:232457008 RGO:32390 laryngeal papillomatosis RGO:32390 RGO:32391 tracheobronchial papillomatosis RGO:32391 DOID:12608 SNOMEDCT:22754005 RGO:32392 staphylococcal pneumonia RGO:32392 DOID:13272 RADLEX:RID34613 RGO:32394 Klebsiella pneumonia RGO:32394 RGO:32395 E. coli pneumonia RGO:32395 ORDO:90066 RGO:32396 Pseudomonas pneumonia RGO:32396 SNOMEDCT:195888009 RGO:32397 Proteus pneumonia RGO:32397 HP:0030250 RGO:32398 pulmonary granulomatosis RGO:32398 RGO:32399 eosinophilic lung disease RGO:32399 RGO:32400 injection of foreign material RGO:32400 RGO:32401 subphrenic neoplasm RGO:32401 RGO:32402 perforation by venous catheter RGO:32402 RGO:32403 lung blastoma RGO:32403 DOID:2784 RGO:32404 lung sarcoma RGO:32404 ICD10CM:K22.3 SNOMEDCT:23387001 RGO:32405 perforation of esophagus RGO:32405 SNOMEDCT:235674005 RGO:32406 perforation of stomach RGO:32406 SNOMEDCT:713582000 RGO:32407 malignant germ cell neoplasm RGO:32407 DOID:850 HP:0002088 RGO:32408 lung disease RGO:32408 RGO:32409 acute aspiration RGO:32409 RGO:32410 opportunistic pneumonia RGO:32410 RGO:32411 lymphangitic metastasis RGO:32411 RGO:32412 congenital esophageal lung RGO:32412 DOID:0050870 RGO:32413 bronchioalveolar carcinoma RGO:32413 RGO:32414 traumatic lung collapse RGO:32414 RGO:32415 postoperative lung collapse RGO:32415 RGO:32416 idiopathic aspiration pneumonia RGO:32416 DOID:13137 RGO:32418 Werdnig-Hoffman disease RGO:32418 RGO:32419 congenital laryngeal wall deficiency RGO:32419 HP:0008751 RGO:32420 laryngotracheal cleft RGO:32420 DOID:12375 SNOMEDCT:396285007 RGO:32421 bronchopneumonia RGO:32421 DOID:10532 SNOMEDCT:34020007 RGO:32422 streptococcal pneumonia RGO:32422 HP:0004960 RGO:32423 absent pulmonary artery RGO:32423 RGO:32424 pulmonary artery occlusion RGO:32424 RGO:32425 pulmonary arterial thromboembolism RGO:32425 HP:0004971 ORDO:99083 SNOMEDCT:54682008 RGO:32427 pulmonary artery hypoplasia RGO:32427 RGO:32428 idiopathic pulmonary edema RGO:32428 RGO:32429 systemic-pulmonary artery shunt RGO:32429 RGO:32432 rapid reexpansion of lung RGO:32432 RGO:32433 prolonged lateral decubitus position RGO:32433 RADLEX:RID4635 SNOMEDCT:3821009 SNOMEDCT:425359009 RGO:32434 blunt injury RGO:32434 ICD10CM:J86.0 RGO:32435 pleural fistula RGO:32435 RGO:32436 gastric-pleural fistula RGO:32436 RGO:32437 esophageal-pleural fistula RGO:32437 SNOMEDCT:116656002 SNOMEDCT:387039007 RGO:32439 bromocriptine RGO:32439 SNOMEDCT:55680006 RGO:32441 drug overdose RGO:32441 RGO:32442 rapid lung re-expansion RGO:32442 RGO:32443 contraction atelectasis RGO:32443 RGO:32444 fractured bronchus RGO:32444 RGO:32445 stricture of bronchus RGO:32445 RGO:32447 foreign body aspiration RGO:32447 RGO:32449 lung hamartoma RGO:32449 RGO:32450 lung myoblastoma RGO:32450 RGO:32452 postoperative adhesive atelectasis RGO:32452 relaxation atelectasis SNOMEDCT:16537000 RGO:32453 compression atelectasis RGO:32453 RGO:32456 diaphragmatic elevation RGO:32456 RGO:32457 peripheral mucous plugs RGO:32457 SNOMEDCT:54304004 RGO:32460 bulbar paralysis RGO:32460 SNOMEDCT:385479009 RGO:32462 follicular bronchiolitis RGO:32462 RGO:32463 viral bronchopneumonia RGO:32463 RGO:32464 mycoplasma bronchopneumonia RGO:32464 RGO:32465 bacterial bronchopneumonia RGO:32465 RGO:32466 Aspergillus bronchopneumonia RGO:32466 RGO:32468 peribronchovascular lung nodules RGO:32468 RGO:32469 septal lung nodules RGO:32469 RGO:32470 subpleural lung nodules RGO:32470 RGO:32473 old granulomatous disease RGO:32473 RGO:32474 respiratory bronchiolitis RGO:32474 RGO:32475 cellular bronchiolitis RGO:32475 RGO:32476 infectious bronchiolitis RGO:32476 RGO:32477 panbronchiolitis RGO:32477 DOID:2670 SNOMEDCT:44342003 RGO:32480 transitional papilloma RGO:32480 RADLEX:RID4265 SNOMEDCT:109355002 SNOMEDCT:68956006 RGO:32481 carcinoma in situ RGO:32481 RADLEX:RID4260 RGO:32482 spindle cell squamous carcinoma RGO:32482 DOID:0070003 DOID:4766 SNOMEDCT:86049000 RGO:32483 blastoma RGO:32483 RGO:32484 infected bulla RGO:32484 RGO:32485 complicated hydatid cyst RGO:32485 RGO:32494 bowel pseudo-obstruction RGO:32494 RGO:32495 corona sign RGO:32495 RGO:32497 lung laceration RGO:32497 RGO:32501 lung gangrene RGO:32501 RGO:32502 angioinvasive fungal disease RGO:32502 SNOMEDCT:8672004 RGO:32504 Coccidioides RGO:32504 DOID:12608 RGO:32506 Staphylococcus aureus pneumonia RGO:32506 RGO:32507 bronchial obstruction with distal abscess RGO:32507 RGO:32508 infarcted pneumonia RGO:32508 RGO:32509 lung hematoma RGO:32509 RGO:32510 lung abscesses RGO:32510 RGO:32511 pulmonary arterial coarctation RGO:32511 RGO:32512 fluid-filled bronchiectatic cysts RGO:32512 RGO:32513 hamartomas RGO:32513 RGO:32514 focal pleural thickening RGO:32514 loculated pleural effusions loculated pleural fluid SNOMEDCT:427895005 RGO:32515 loculated pleural effusion RGO:32515 RADLEX:RID1744 RGO:32517 kidney surgery RGO:32517 RGO:32518 CABG RGO:32518 RGO:32519 thoracic duct ligation RGO:32519 RGO:32520 thoracic duct injury RGO:32520 RGO:32521 mediastinal mass with lymphatic obstruction RGO:32521 DOID:849 SNOMEDCT:398726004 RGO:32522 rheumatoid lung RGO:32522 RGO:32523 lymphangitic spread of tumor RGO:32523 RGO:32527 pulmonary venous obstruction RGO:32527 RGO:32528 peripheral arterial-venous malformation RGO:32528 RGO:32530 intermediate-stage cementoblastoma RGO:32530 RGO:32531 root canal cement RGO:32531 RGO:32532 complex and compound odontoma RGO:32532 RGO:32533 nodular cemental mass RGO:32533 RGO:32534 complex or compound odontoma RGO:32534 RGO:32535 retained deciduous tooth root RGO:32535 RGO:32536 infected residual permanent root tip RGO:32536 RGO:32537 pyogenic osteomyelitis with sequestrum RGO:32537 HP:0011069 SNOMEDCT:266414008 SNOMEDCT:367534004 RGO:32538 supernumerary tooth RGO:32538 HP:0000706 SNOMEDCT:278658009 RGO:32539 unerupted tooth RGO:32539 RGO:32540 fibrosis of alveolar mucosa RGO:32540 ICD10CM:K00.4 SNOMEDCT:35452009 RGO:32541 dilaceration of tooth RGO:32541 RGO:32542 jaw fracture RGO:32542 RGO:32543 disorientation of tooth germ RGO:32543 RGO:32544 ectopic tooth eruption RGO:32544 RADLEX:RID4181 SNOMEDCT:84983008 RGO:32546 ameloblastic fibro-odontoma RGO:32546 SNOMEDCT:235734008 RGO:32551 small bowel fistula RGO:32551 RGO:32552 peripheral mucous plug RGO:32552 RGO:32553 lobar atelectasis RGO:32553 RGO:32554 segmental atelectasis RGO:32554 RGO:32558 acinar lung nodule RGO:32558 RGO:32559 bat wing distribution in lung RGO:32559 RGO:32562 nodule with ill-defined margin RGO:32562 RGO:32563 peribronchiolar nodule RGO:32563 RGO:32564 perihilar lung opacity RGO:32564 RGO:32565 diffuse distribution RGO:32565 RGO:32566 diffuse lung opacity RGO:32566 RGO:32567 segmental lung opacity RGO:32567 RGO:32568 lobar lung opacity RGO:32568 RADLEX:RID28494 SNOMEDCT:448370006 RGO:32569 round atelectasis RGO:32569 RGO:32570 localized pulmonary edema RGO:32570 RGO:32571 lung torsion RGO:32571 RGO:32573 infectious pneumonia RGO:32573 Aspergillus hypersensitivity RGO:32575 hypersensitivity aspergillosis RGO:32575 MPS 3 mucopolysaccharidosis type 3 SNOMEDCT:88393000 RGO:32576 Sanfilippo syndrome RGO:32576 RADLEX:RID49619 SNOMEDCT:68790008 RGO:32577 amyloid RGO:32577 SNOMEDCT:25889007 RGO:32578 xanthofibroma RGO:32578 central chondrosarcoma classical chondrosarcoma RGO:32579 medullary chondrosarcoma RGO:32579 RADLEX:RID4144 SNOMEDCT:128776008 RGO:32582 dedifferentiated chondrosarcoma RGO:32582 DOID:5861 RADLEX:RID4145 SNOMEDCT:75622000 RGO:32583 myxoid chondrosarcoma RGO:32583 RGO:32584 squamous cell skin cancer RGO:32584 RGO:32586 protein-deficient state RGO:32586 RGO:32587 central cavernous hemangioma RGO:32587 RGO:32588 squamous cell carcinoma of mandible RGO:32588 RGO:32589 chronic anticonvulsant therapy RGO:32589 RGO:32590 focal osteoporotic marrow defects RGO:32590 RGO:32591 postextraction tooth sockets RGO:32591 RGO:32592 nodular cemental masses RGO:32592 hemorrhagic bone cyst SNOMEDCT:112643007 RGO:32593 traumatic bone cyst RGO:32593 RGO:32595 disease extension from adjacent tooth RGO:32595 RGO:32596 advanced periodontal disease RGO:32596 RGO:32597 iatrogenic perforation of root of tooth RGO:32597 RGO:32598 benign nonodontogenic tumor RGO:32598 RGO:32599 primary tooth crypt RGO:32599 RADLEX:RID9266 RGO:32601 incisive foramen RGO:32601 RGO:32602 lateral fossa between lateral incisor and canine teeth RGO:32602 RGO:32603 bone marrow pattern RGO:32603 SNOMEDCT:70687006 RGO:32604 nutrient canal RGO:32604 RGO:32605 mental canal RGO:32605 RADLEX:RID9504 SNOMEDCT:244686000 RGO:32606 mental foramen RGO:32606 RGO:32607 globulomaxillary radiolucency RGO:32607 RGO:32608 lateral canal periapical cyst RGO:32608 ICD10CM:K09.0 SNOMEDCT:88477005 RGO:32609 lateral periodontal cyst RGO:32609 RGO:32610 central hemangioma RGO:32610 RGO:32611 immature odontoma RGO:32611 RGO:32614 soft-tissue deformity RGO:32614 SNOMEDCT:23979009 RGO:32615 pleurectomy RGO:32615 RGO:32616 plombage RGO:32616 RGO:32617 metastasis to chest wall RGO:32617 SNOMEDCT:94602001 RGO:32619 metastasis to spine RGO:32619 RGO:32622 fluid-filled bulla RGO:32622 RGO:32623 fluid-filled adenomatoid malformation RGO:32623 RGO:32624 adenomatoid malformation RGO:32624 RGO:32625 fluid-filled bronchial cyst RGO:32625 RGO:32626 fluid-filled bronchiectatic cyst RGO:32626 RGO:32627 benign lung neoplasm RGO:32627 RGO:32628 normal pulmonary blood vessel RGO:32628 SNOMEDCT:128585006 SNOMEDCT:199113001 RGO:32629 anomalous pulmonary vein RGO:32629 RGO:32630 postinflammatory scar RGO:32630 RADLEX:RID1496 SNOMEDCT:196662004 RGO:32631 intrapulmonary lymph node RGO:32631 DOID:10325 RADLEX:RID5344 SNOMEDCT:805002 RGO:32632 silicosis RGO:32632 SNOMEDCT:90540004 RGO:32633 Dirofilaria immitis RGO:32633 RGO:32634 atypical viral pneumonia RGO:32634 DOID:10531 SNOMEDCT:233607000 RGO:32635 pneumococcal pneumonia RGO:32635 RGO:32639 extraabdominal desmoid tumor RGO:32639 RADLEX:RID4291 SNOMEDCT:47284001 RGO:32640 aggressive fibromatosis RGO:32640 ICD10CM:K44.0 RGO:32641 incarcerated diaphragmatic hernia RGO:32641 RGO:32642 thoracoabdominal liposarcoma RGO:32642 RGO:32643 thoracoabdominal lipoma RGO:32643 RGO:32645 ruptured diaphragm RGO:32645 RGO:32646 abdominal neoplasm RGO:32646 SNOMEDCT:257353006 RGO:32647 ventriculopleural shunt RGO:32647 RGO:32648 malplaced intravenous catheter RGO:32648 RGO:32649 postpneumonectomy empyema RGO:32649 RGO:32650 thoracic extension of neck abscess RGO:32650 RGO:32651 renal surgery RGO:32651 DOID:4962 ICD10CM:A18.84 SNOMEDCT:67256000 RGO:32652 tuberculous pericarditis RGO:32652 RGO:32653 metastatic pericarditis RGO:32653 SNOMEDCT:233813006 RGO:32654 ventilator lung RGO:32654 RGO:32655 drug-induced pulmonary disease RGO:32655 RGO:32656 chest wall sarcoma RGO:32656 RGO:32658 mediastinal fat deposition RGO:32658 RGO:32660 rebound hyperplasia RGO:32660 RGO:32661 cervical aorta RGO:32661 HP:0005113 RGO:32662 aortic arch aneurysm RGO:32662 RGO:32663 brachiocephalic vessel elongation RGO:32663 RGO:32664 brachiocephalic vessel ectasia RGO:32664 RGO:32667 brachiocephalic artery buckling RGO:32667 RGO:32668 brachiocephalic artery dilatation RGO:32668 RGO:32669 idiopathic fibrosing mediastinitis RGO:32669 RGO:32670 dilated thoracic duct RGO:32670 SNOMEDCT:359672006 RGO:32672 median sternotomy RGO:32672 HP:0006539 RGO:32676 bronchial cartilage hypoplasia RGO:32676 RGO:32677 bronchial chondromalacia RGO:32677 RGO:32678 absent bronchial cartilage RGO:32678 RGO:32679 funnel breast RGO:32679 RGO:32680 pleuropericardial adhesion RGO:32680 RGO:32681 postinfarction myocardial scar RGO:32681 HP:0031457 RGO:32683 pulmonary opacity RGO:32683 RGO:32684 chest wall hematoma RGO:32684 RGO:32685 cystic adenomatoid malformation type 3 RGO:32685 RGO:32686 unilateral lung consolidation RGO:32686 RGO:32687 pulmonary mass RGO:32687 RGO:32688 cystic thymoma RGO:32688 RGO:32691 cyanotic admixture lesion RGO:32691 RGO:32692 truncus arteriosus type 1 RGO:32692 RGO:32693 talc inhalation RGO:32693 RGO:32694 bauxite inhalation RGO:32694 SNOMEDCT:63606002 RGO:32695 tin oxide RGO:32695 rutile SNOMEDCT:432929006 SNOMEDCT:62036000 RGO:32696 titanium dioxide RGO:32696 RADLEX:RID11826 SNOMEDCT:413576005 SNOMEDCT:47809000 RGO:32698 arsenic RGO:32698 RGO:32699 chromate RGO:32699 RADLEX:RID11944 SNOMEDCT:40584000 RGO:32700 uranium RGO:32700 RADLEX:RID11940 SNOMEDCT:7269004 RGO:32701 thorium RGO:32701 RGO:32702 plutonium inhalation RGO:32702 RGO:32703 radioactive ore RGO:32703 RGO:32704 radon inhalation RGO:32704 SNOMEDCT:25419009 SNOMEDCT:396014007 RGO:32705 barium sulfate RGO:32705 RADLEX:RID11876 SNOMEDCT:281207004 RGO:32706 cerium RGO:32706 RADLEX:RID11854 SNOMEDCT:371257001 SNOMEDCT:406951002 SNOMEDCT:41967008 RGO:32707 silver RGO:32707 RGO:32708 argyrosiderosis RGO:32708 RGO:32709 kaolin inhalation RGO:32709 RGO:32710 tungsten carbide RGO:32710 RGO:32713 recurrent lung cancer RGO:32713 RADLEX:RID4867 SNOMEDCT:360371003 RGO:32714 cardiogenic pulmonary edema RGO:32714 RGO:32715 leukoagglutination RGO:32715 RGO:32716 noncardiogenic pulmonary edema RGO:32716 SNOMEDCT:80771008 RGO:32718 Rhodococcus equi RGO:32718 HP:0003270 SNOMEDCT:60728008 RGO:32720 abdominal distention RGO:32720 RGO:32721 inspiratory airway obstruction RGO:32721 RGO:32722 maternal oversedation RGO:32722 DOID:6132 HP:0012388 ICD10CM:J20 SNOMEDCT:10509002 RGO:32723 acute bronchitis RGO:32723 RGO:32724 high-concentration oxygen RGO:32724 SNOMEDCT:91424007 RGO:32725 nitrogen dioxide RGO:32725 RGO:32726 silo-filler disease RGO:32726 SNOMEDCT:409378005 SNOMEDCT:6710000 RGO:32727 nitric oxide RGO:32727 RGO:32730 primary tumor RGO:32730 RGO:32733 metastatic tumor RGO:32733 RGO:32735 chest tumor in infant RGO:32735 RGO:32736 chest tumor in child RGO:32736 RGO:32737 chest tumor in adolescent RGO:32737 SNOMEDCT:425265006 RGO:32740 knife wound RGO:32740 HP:0031649 RGO:32742 aortic rupture RGO:32742 RGO:32743 pulmonary hematoma RGO:32743 RGO:32744 leukemia in a child RGO:32744 RGO:32745 lymphoma in a child RGO:32745 RGO:32746 neuroblastoma in a child RGO:32746 RGO:32747 prostate carcinoma in an adult RGO:32747 RGO:32748 gastrointestinal carcinoma in an adult RGO:32748 RGO:32749 fibrous-type ameloblastoma RGO:32749 RGO:32751 fibrous dysplasia Jaffe-Lichtenstein type RGO:32751 RGO:32752 intramuscular myxomas RGO:32752 DOID:2998 HP:0010788 RADLEX:RID45690 RGO:32753 testicular cancer RGO:32753 RGO:32754 gastrointestinal tract carcinoma RGO:32754 SNOMEDCT:31104000 RGO:32756 benign hemangioendothelioma RGO:32756 RGO:32757 tranquilizer therapy RGO:32757 SNOMEDCT:19595005 SNOMEDCT:398955002 RGO:32758 phenolphthalein RGO:32758 SNOMEDCT:37400007 SNOMEDCT:387202002 RGO:32759 magnesium sulfate RGO:32759 RGO:32760 pseudovitamin D-deficiency osteomalacia RGO:32760 RGO:32761 pseudovitamin D-deficiency rickets RGO:32761 ICD10CM:E74.12 ORDO:469 SNOMEDCT:20052008 RGO:32762 hereditary fructose intolerance RGO:32762 RGO:32763 maternal osteomalacia RGO:32763 RGO:32764 aluminum hydroxide hemodialysis RGO:32764 RGO:32766 aluminum-based antacid therapy RGO:32766 SNOMEDCT:238119005 RGO:32767 phosphate deficiency RGO:32767 HP:0003109 RGO:32768 phosphaturia RGO:32768 HP:0003076 ICD10CM:R81 SNOMEDCT:45154002 RGO:32769 glycosuria RGO:32769 RGO:32770 diphosphonate treatment RGO:32770 ICD10CM:M83.0 SNOMEDCT:190643008 RGO:32771 puerperal osteomalacia RGO:32771 RGO:32773 excessive calcium excretion via placenta RGO:32773 RGO:32774 excessive calcium excretion via breast RGO:32774 RGO:32775 excessive phosphorus excretion via breast RGO:32775 RGO:32776 excessive phosphorus excretion via placenta RGO:32776 SNOMEDCT:276702002 RGO:32777 neonatal rickets RGO:32777 RGO:32779 impaired hepatic hydroxylation of vitamin D RGO:32779 RADLEX:RID1627 RGO:32780 gastric resection RGO:32780 RGO:32781 small bowel bypass RGO:32781 DOID:10573 HP:0002749 RADLEX:RID5391 SNOMEDCT:4598005 RGO:32782 osteomalacia RGO:32782 DOID:10609 HP:0002748 RADLEX:RID34716 SNOMEDCT:41345002 RGO:32783 rickets RGO:32783 DOID:693 HP:0006297 SNOMEDCT:26597004 RGO:32788 enamel hypoplasia RGO:32788 RGO:32790 irregular tooth placement RGO:32790 HP:0000695 RGO:32791 neonatal teeth RGO:32791 RGO:32792 irregular spacing RGO:32792 RGO:32793 peglike incisors RGO:32793 HP:0006485 RGO:32794 missing incisors RGO:32794 RGO:32795 irregular placement RGO:32795 RGO:32796 persistent deciduous teeth RGO:32796 HP:0006297 SNOMEDCT:699421005 RGO:32797 enamel dysplasia RGO:32797 HP:0000692 RGO:32798 malaligned teeth RGO:32798 RADLEX:RID4753 SNOMEDCT:408737001 RGO:32799 malposition RGO:32799 RGO:32800 small malaligned teeth RGO:32800 RGO:32801 thin enamel RGO:32801 RGO:32803 progressive tooth mobility and fracture RGO:32803 DOID:11121 ICD10CM:K04.0 SNOMEDCT:32620007 RGO:32804 pulpitis RGO:32804 HP:0006480 RGO:32806 early tooth loss RGO:32806 RGO:32807 defective dentition RGO:32807 SNOMEDCT:5639000 RGO:32808 delayed dentition RGO:32808 juxtacortical myositis ossificans RGO:32809 parosteal myositis ossificans RGO:32809 RGO:32810 healing stress fracture RGO:32810 PAPVC PAPVR partial APVC partial APVR partial anomalous pulmonary venous connection HP:0010773 ICD10CM:Q26.3 ORDO:99124 RADLEX:RID34766 SNOMEDCT:68237008 RGO:32814 partial anomalous pulmonary venous return RGO:32814 HP:0001694 RADLEX:RID4972 RGO:32821 right-to-left shunt RGO:32821 RGO:32822 descending aorta aneurysm RGO:32822 RGO:32823 thoracic duct cyst RGO:32823 RGO:32824 loculated hemothorax RGO:32824 RGO:32825 metastatic bronchogenic carcinoma RGO:32825 RGO:32827 extension of retroperitoneal mass RGO:32827 RADLEX:RID3725 RGO:32828 spinal tuberculosis RGO:32828 RGO:32829 suppurative spondylitis RGO:32829 RGO:32830 intrathoracic thyroid tumor RGO:32830 SNOMEDCT:427898007 RGO:32831 dental infection RGO:32831 RGO:32832 heart trauma RGO:32832 RGO:32833 aorta trauma RGO:32833 RGO:32834 great vessel trauma RGO:32834 SNOMEDCT:128601007 RGO:32835 lung infection RGO:32835 RGO:32836 pleural infection RGO:32836 RGO:32837 ruptured lymphangioma RGO:32837 RGO:32838 catheter malposition RGO:32838 NIPF RGO:32840 nonspecific interstitial pulmonary fibrosis RGO:32840 BCNU bis-chloroethylnitrosourea SNOMEDCT:387281007 SNOMEDCT:51326002 RGO:32842 carmustine RGO:32842 RGO:32847 lymphangitic lung metastasis RGO:32847 SNOMEDCT:234062003 RGO:32848 pulmonary vein stenosis RGO:32848 RGO:32849 large bulla RGO:32849 RADLEX:RID49910 SNOMEDCT:172043006 SNOMEDCT:69031006 RGO:32850 mastectomy RGO:32850 RGO:32851 pectoral muscle atrophy RGO:32851 RGO:32852 idiopathic radioulnar synostosis RGO:32852 RGO:32853 Nievergelt-Pearlman syndrome RGO:32853 RGO:32854 chronic aspiration pneumonia RGO:32854 type 2 aortic arch RGO:32857 right posterior aortic arch RGO:32857 type 1 aortic arch RGO:32859 right anterior aortic arch RGO:32859 RGO:32861 mirror-image branching of great arteries RGO:32861 RGO:32863 prosthetic aortic valve dysfunction RGO:32863 RGO:32866 heart incision RGO:32866 SNOMEDCT:232717009 RGO:32867 coronary artery bypass graft RGO:32867 RGO:32869 calcification in great vessels RGO:32869 RGO:32870 calcification in heart RGO:32870 SNOMEDCT:66205002 RGO:32871 injection of gas RGO:32871 RGO:32872 cerebral pneumography RGO:32872 RADLEX:RID10373 SNOMEDCT:33148003 RGO:32873 arthrography RGO:32873 RGO:32875 attempted suicide RGO:32875 RGO:32876 attempted homicide RGO:32876 RGO:32877 paranasal sinus irrigation RGO:32877 RGO:32878 abscess drainage RGO:32878 RGO:32879 percutaneous high-pressure injection RGO:32879 RGO:32880 air hose injection RGO:32880 RGO:32881 artificial pneumoperitoneum RGO:32881 SNOMEDCT:29068008 RGO:32882 artificial pneumothorax RGO:32882 RGO:32883 neoplastic vascular invasion RGO:32883 RGO:32884 bronchovascular fistula RGO:32884 RGO:32885 esophageal-aortic fistula RGO:32885 RGO:32886 cardiac bypass RGO:32886 RGO:32887 lung resection RGO:32887 RGO:32888 abdominal aortic graft RGO:32888 SNOMEDCT:429446009 RGO:32889 vascular catheterization RGO:32889 SNOMEDCT:14152002 SNOMEDCT:385228000 RGO:32890 intravenous infusion RGO:32890 RADLEX:RID10371 SNOMEDCT:77343006 RGO:32891 angiography RGO:32891 RGO:32892 cystic medial necrosis of aorta RGO:32892 RGO:32893 aortic nipple RGO:32893 RGO:32894 circumflex left aortic arch with right descending aorta RGO:32894 RGO:32895 cervical left aortic arch with right descending aorta RGO:32895 RGO:32896 unilateral air trapping RGO:32896 RGO:32897 bronchial foreign body RGO:32897 DOID:3906 HP:0030077 RGO:32898 bronchial neoplasm RGO:32898 RGO:32900 improper radiographic position RGO:32900 RGO:32901 pulmonary aplasia RGO:32901 SNOMEDCT:86252004 RGO:32902 congenital absence of pulmonary artery RGO:32902 RGO:32903 unilateral central pulmonary artery obstruction RGO:32903 RGO:32904 thymus of normal infant RGO:32904 RGO:32906 pericardial lipoma RGO:32906 RGO:32907 posterior dislocation of medial clavicle RGO:32907 RGO:32910 subcarinal lymphadenopathy RGO:32910 RGO:32911 paraesophageal lymphadenopathy RGO:32911 HP:0100002 RGO:32912 pleural mesothelioma RGO:32912 HP:0100750 SNOMEDCT:46621007 RGO:32913 pulmonary atelectasis RGO:32913 RGO:32914 traumatic tracheal rupture RGO:32914 RGO:32915 traumatic bronchial rupture RGO:32915 RGO:32916 osteomyelitis of sternum RGO:32916 RGO:32917 endoscopic trauma RGO:32917 SNOMEDCT:235197007 RGO:32918 dilatation of esophageal stricture RGO:32918 SNOMEDCT:233734006 RGO:32919 acute mediastinitis RGO:32919 SNOMEDCT:42522007 RGO:32920 mediastinal abscess RGO:32920 RGO:32923 broken pacemaker wire RGO:32923 RGO:32924 central line catheter RGO:32924 RGO:32925 ventriculo-atrial shunt RGO:32925 SNOMEDCT:174814003 RGO:32926 repair of tetralogy of Fallot RGO:32926 RGO:32928 3-M syndrome 3M1 RGO:32928 RGO:32929 3-M syndrome 3M2 RGO:32929 ORDO:93298 RGO:32930 achondrogenesis type 1B RGO:32930 ORDO:968 RGO:32932 acromesomelic dysplasia Hunter-Thompson type RGO:32932 RGO:32933 acromesomelic dysplasia Osebold-Remondini type RGO:32933 DOID:3413 ORDO:61 RGO:32938 alpha-mannosidosis RGO:32938 RGO:32940 Antley-Bixler variant caused by FGFR2 mutation RGO:32940 DOID:3633 ORDO:118 RGO:32942 beta-mannosidosis RGO:32942 DOID:0110975 ORDO:140908 RGO:32943 brachydactyly type B2 RGO:32943 RGO:32944 brachydactyly with anonychia RGO:32944 ORDO:1275 RGO:32945 brachydactyly with elbow dysplasia RGO:32945 ORDO:1276 RGO:32946 brachydactyly-hypertension syndrome RGO:32946 RGO:32947 brachydactyly-mental retardation syndrome RGO:32947 ORDO:93304 RGO:32948 brachyolmia autosomal dominant type RGO:32948 brachyolmia Hobaek type ORDO:93303 RGO:32949 brachyolmia Toledo type RGO:32949 RGO:32950 Bruck syndrome type 1 RGO:32950 RGO:32951 Bruck syndrome type 2 RGO:32951 RGO:32953 Caffey disease severe variants with prenatal onset RGO:32953 RGO:32954 calcium pyrophosphate deposition disease type 2 RGO:32954 RGO:32956 Cenani-Lenz like syndactyly RGO:32956 ORDO:99647 RGO:32957 cheiro-spondyloenchondromatosis RGO:32957 ORDO:2025 SNOMEDCT:389273002 RGO:32958 cherubism with gingival fibromatosis RGO:32958 RGO:32961 chronic recurrent multifocal osteomyelitis with congenital dyserythropoietic anemia RGO:32961 RGO:32964 costo-vertebral segmentation defect with mesomelia RGO:32964 RGO:32965 cranioectodermal dysplasia type 1 RGO:32965 RGO:32966 cranioectodermal dysplasia type 2 RGO:32966 ORDO:1541 RGO:32967 craniosynostosis Boston type RGO:32967 Muenke syndrome ORDO:53271 RGO:32968 craniosynostosis Muenke type RGO:32968 RGO:32969 craniosynostosis with cutis gyrata RGO:32969 RGO:32970 cutis laxa autosomal recessive form type 2A RGO:32970 RGO:32971 cutis laxa autosomal recessive form type 2B RGO:32971 RGO:32972 Desbuquois dysplasia other variants with or without accessory ossification center RGO:32972 RGO:32973 Desbuquois dysplasia with accessory ossification center in digit 2 RGO:32973 RGO:32974 Desbuquois dysplasia with short metacarpals and elongated phalanges RGO:32974 RGO:32977 ectrodactyly - ectodermal dysplasia - cleft palate syndrome type 1 RGO:32977 RGO:32978 ectrodactyly - ectodermal dysplasia - cleft palate syndrome type 3 RGO:32978 RGO:32980 Ehlers-Danlos syndrome CHST14 type RGO:32980 RGO:32984 familial hypocalciuric hypercalcemia with transient neonatal hyperparathyroidism RGO:32984 ORDO:251262 SNOMEDCT:715899006 RGO:32985 familial osteochondritis dissecans RGO:32985 RGO:32989 fibulin1-associated complex synpolydactyly RGO:32989 RGO:32991 frontonasal dysplasia type 1 RGO:32991 RGO:32992 frontonasal dysplasia type 2 RGO:32992 RGO:32993 frontonasal dysplasia type 3 RGO:32993 RGO:32995 geleophysic dysplasia other types RGO:32995 SNOMEDCT:38494008 RGO:32998 homozygous dyschondrosteosis RGO:32998 ORDO:247676 RGO:33002 hypophosphatasia adult form RGO:33002 RGO:33003 hypophosphatasia perinatal lethal and infantile forms RGO:33003 ORDO:89937 RGO:33004 hypophosphatemic rickets autosomal dominant RGO:33004 RGO:33005 hypophosphatemic rickets autosomal recessive type 1 RGO:33005 RGO:33006 hypophosphatemic rickets autosomal recessive type 2 RGO:33006 RGO:33007 hypophosphatemic rickets with hypercalciuria autosomal recessive RGO:33007 RGO:33008 hypophosphatemic rickets with hypercalciuria X-linked recessive RGO:33008 SNOMEDCT:254067002 RGO:33010 immuno-osseous dysplasia RGO:33010 ORDO:2028 SNOMEDCT:238861002 RGO:33011 juvenile hyaline fibromatosis RGO:33011 HRD syndrome KCS1 Kenny-Caffey syndrome type 1 Middle-East syndrome Richadson-Kirk syndrome SSS Sanjad-Sakati syndrome hypoparathyroidism-retardation-dysmophic syndrome hypoparathyroidism-retardation-dysmorphism syndrome RGO:33012 Kenny-Caffey dysplasia type 1 RGO:33012 RGO:33013 Kenny-Caffey dysplasia type 2 RGO:33013 RGO:33014 Klippel-Feil anomaly with laryngeal malformation RGO:33014 ORDO:503 RGO:33016 Larsen syndrome dominant RGO:33016 RGO:33017 late-onset spondyloepiphyseal dysplasia autosomal recessive type RGO:33017 RGO:33019 mandibuloacral dysplasia type A RGO:33019 RGO:33020 mandibuloacral dysplasia type B RGO:33020 RGO:33022 Meckel syndrome type 1 RGO:33022 RGO:33023 Meckel syndrome type 2 RGO:33023 RGO:33024 Meckel syndrome type 3 RGO:33024 RGO:33025 Meckel syndrome type 4 RGO:33025 RGO:33026 Meckel syndrome type 5 RGO:33026 RGO:33027 Meckel syndrome type 6 RGO:33027 ORDO:1879 RGO:33028 melorheostosis with osteopoikilosis RGO:33028 RGO:33029 mesomelic dysplasia Korean type RGO:33029 RGO:33030 mesomelic dysplasia Kozlowski-Reardon type RGO:33030 ORDO:85170 SNOMEDCT:715652002 RGO:33031 mesomelic dysplasia Savarirayan type RGO:33031 RGO:33032 mesomelic dysplasia with acral synostoses RGO:33032 RGO:33033 metaphyseal anadysplasia type 1 RGO:33033 RGO:33034 metaphyseal anadysplasia type 2 RGO:33034 ORDO:85188 RGO:33035 metaphyseal dysplasia Braun-Tinschert type RGO:33035 ORDO:2501 RGO:33038 metaphyseal dysplasia Spahr type RGO:33038 RGO:33039 metaphyseal dysplasia with pancreatic insufficiency and cyclic neutropenia RGO:33039 ORDO:2636 RGO:33040 microcephalic osteodysplastic primordial dwarfism type 1/3 RGO:33040 ORDO:93279 SNOMEDCT:389159004 RGO:33042 mild spondyloepiphyseal dysplasia with premature onset arthrosis RGO:33042 RGO:33044 mirror-image polydactyly of hands and feet RGO:33044 DOID:0110973 RGO:33045 Mononen type brachydactyly RGO:33045 RGO:33046 mucolipidosis II alpha/beta type RGO:33046 RGO:33047 mucolipidosis III alpha/beta type RGO:33047 RGO:33048 mucolipidosis III gamma type RGO:33048 Sanfilippo syndrome type A RGO:33050 mucopolysaccharidosis type 3A RGO:33050 Sanfilippo syndrome type B RGO:33051 mucopolysaccharidosis type 3B RGO:33051 Sanfilippo syndrome type C RGO:33052 mucopolysaccharidosis type 3C RGO:33052 Sanfilippo syndrome type D RGO:33053 mucopolysaccharidosis type 3D RGO:33053 ORDO:2774 RGO:33054 multicentric carpal-tarsal osteolysis with and without nephropathy RGO:33054 RGO:33055 multiple cartilaginous exostoses 1 RGO:33055 RGO:33056 multiple cartilaginous exostoses 2 RGO:33056 RGO:33057 multiple cartilaginous exostoses 3 RGO:33057 RGO:33058 multiple epiphyseal dysplasia autosomal recessive type RGO:33058 RGO:33059 multiple epiphyseal dysplasia other types RGO:33059 ORDO:93308 SNOMEDCT:715673002 RGO:33060 multiple epiphyseal dysplasia type 1 RGO:33060 RGO:33061 multiple epiphyseal dysplasia type 2 RGO:33061 RGO:33062 multiple epiphyseal dysplasia type 3 RGO:33062 ORDO:93311 SNOMEDCT:715674008 RGO:33063 multiple epiphyseal dysplasia type 5 RGO:33063 RGO:33064 multiple epiphyseal dysplasia type 6 RGO:33064 RGO:33065 multiple epiphyseal dysplasia with microcephaly and nystagmus RGO:33065 RGO:33066 multiple synostoses syndrome type 1 RGO:33066 RGO:33067 multiple synostoses syndrome type 2 RGO:33067 RGO:33068 multiple synostoses syndrome type 3 RGO:33068 ORDO:417 RGO:33069 neonatal hyperparathyroidism severe form RGO:33069 RGO:33070 neonatal Schwartz-Jampel syndrome RGO:33070 RGO:33071 oculodentoosseous dysplasia mild type RGO:33071 RGO:33072 oculodentoosseous dysplasia severe type RGO:33072 ORDO:93328 RGO:33073 omodysplasia dominant type RGO:33073 RGO:33077 osteogenesis imperfecta moderate form RGO:33077 RGO:33078 osteogenesis imperfecta non-deforming form RGO:33078 RGO:33079 osteogenesis imperfecta other types RGO:33079 RGO:33080 osteogenesis imperfecta perinatal lethal form RGO:33080 RGO:33081 osteogenesis imperfecta progressively deforming type RGO:33081 RGO:33082 osteogenesis imperfecta with calcification of the interosseous membranes and or hypertrophic callus RGO:33082 RGO:33083 osteopenia with radiolucent lesions of the mandible RGO:33083 RGO:33084 osteopetrosis infantile form osteoclast-poor with immunoglobulin deficiency RGO:33084 RGO:33085 osteopetrosis infantile form with nervous system involvement RGO:33085 DOID:0110938 RGO:33086 osteopetrosis intermediate form OPTA2 RGO:33086 DOID:0110945 RGO:33087 osteopetrosis intermediate form OPTB6 RGO:33087 RGO:33088 osteopetrosis intermediate form osteoclast-poor RGO:33088 RGO:33089 osteopetrosis late-onset form type 1 RGO:33089 RGO:33090 osteopetrosis late-onset form type 2 RGO:33090 RGO:33091 osteopetrosis moderate form with defective leucocyte adhesion RGO:33091 RGO:33092 osteopetrosis severe neonatal or infantile forms OPTB1 RGO:33092 RGO:33093 osteopetrosis severe neonatal or infantile forms OPTB4 RGO:33093 ORDO:85179 RGO:33094 osteopetrosis with infantile neuroaxonal dysplasia RGO:33094 DOID:0110941 ORDO:2785 SNOMEDCT:254122007 RGO:33095 osteopetrosis with renal tubular acidosis RGO:33095 RGO:33096 otospondylomegaepiphyseal dysplasia dominant type RGO:33096 RGO:33097 otospondylomegaepiphyseal dysplasia recessive type RGO:33097 RGO:33098 overgrowth syndrome with 2q37 translocations RGO:33098 RGO:33099 overgrowth syndrome with skeletal dysplasia RGO:33099 RGO:33101 Pfeiffer syndrome FGFR1-related RGO:33101 RGO:33102 Pfeiffer syndrome FGFR2-related RGO:33102 DOID:0090143 RGO:33103 platyspondyly with amelogenesis imperfecta RGO:33103 RGO:33105 preaxial polydactyly type 1 RGO:33105 RGO:33106 preaxial polydactyly type 2 RGO:33106 RGO:33107 preaxial polydactyly type 3 RGO:33107 RGO:33108 preaxial polydactyly type 4 RGO:33108 RGO:33110 proximal symphalangism type 1 RGO:33110 RGO:33111 proximal symphalangism type 2 RGO:33111 RGO:33114 recessive Larsen syndrome RGO:33114 DOID:0110851 ORDO:309789 RGO:33116 rhizomelic chondrodysplasia punctata type 1 RGO:33116 DOID:0110852 ORDO:309796 RGO:33117 rhizomelic chondrodysplasia punctata type 2 RGO:33117 DOID:0110853 ORDO:309803 RGO:33118 rhizomelic chondrodysplasia punctata type 3 RGO:33118 ORDO:3107 RGO:33119 Robinow syndrome dominant type RGO:33119 ORDO:1507 RGO:33120 Robinow syndrome recessive type RGO:33120 SADDAN severe achondroplasia with developmental delay and acanthosis nigricans ORDO:85165 RGO:33122 severe achondroplasia - developmental delay - acanthosis nigricans RGO:33122 RGO:33123 severe spondylometaphyseal dysplasia RGO:33123 RGO:33124 short-rib polydactyly syndrome type 1/3 RGO:33124 short rib-polydactyly syndrome Beemer-Langer type ORDO:93268 RGO:33126 short-rib polydactyly syndrome type 4 RGO:33126 RGO:33131 split hand-foot malformation isolated form type 1 RGO:33131 RGO:33132 split hand-foot malformation isolated form type 2 RGO:33132 RGO:33133 split hand-foot malformation isolated form type 3 RGO:33133 RGO:33134 split hand-foot malformation isolated form type 4 RGO:33134 RGO:33135 split hand-foot malformation isolated form type 5 RGO:33135 RGO:33136 split hand-foot malformation with long bone deficiency type 1 RGO:33136 RGO:33137 split hand-foot malformation with long bone deficiency type 2 RGO:33137 RGO:33138 split hand-foot malformation with long bone deficiency type 3 RGO:33138 RGO:33139 spondylocostal dysostosis type 1 RGO:33139 RGO:33140 spondylocostal dysostosis type 2 RGO:33140 RGO:33141 spondylocostal dysostosis type 3 RGO:33141 RGO:33143 spondylodysplastic Ehlers-Danlos syndrome RGO:33143 RGO:33144 spondyloepimetaphyseal dysplasia Aggrecan type RGO:33144 RGO:33145 spondyloepimetaphyseal dysplasia Matrilin type RGO:33145 ORDO:93356 RGO:33146 spondyloepimetaphyseal dysplasia Missouri type RGO:33146 RGO:33147 spondyloepimetaphyseal dysplasia PAPSS2 type RGO:33147 RGO:33149 spondyloepimetaphyseal dysplasia with joint laxity Beighton type RGO:33149 RGO:33150 spondyloepimetaphyseal dysplasia with joint laxity Hall type RGO:33150 ORDO:93283 RGO:33152 spondyloepiphyseal dysplasia Kimberley type RGO:33152 RGO:33153 spondyloepiphyseal dysplasia tarda X-linked RGO:33153 RGO:33154 spondyloepiphyseal dysplasia with metatarsal shortening RGO:33154 ORDO:93316 RGO:33157 spondylometaphyseal dysplasia Schmidt type RGO:33157 RGO:33158 spondylometaphyseal dysplasia Sutcliffe type RGO:33158 ORDO:85167 RGO:33159 spondylometaphyseal dysplasia with cone-rod dystrophy RGO:33159 RGO:33160 spondylometaphyseal dysplasia with retinal degeneration axial type RGO:33160 RGO:33161 spondylometaphyseal dysplasia with severe genu valgum RGO:33161 RGO:33164 Stickler syndrome reccesive type RGO:33164 ORDO:90653 RGO:33165 Stickler syndrome type 1 RGO:33165 ORDO:90654 RGO:33166 Stickler syndrome type 2 RGO:33166 RGO:33168 syndactyly Malik-Percin type RGO:33168 ORDO:93402 SNOMEDCT:715723008 RGO:33169 syndactyly type 1 RGO:33169 ORDO:93406 RGO:33171 syndactyly type 5 RGO:33171 RGO:33172 syndactyly with craniosynostosis RGO:33172 RGO:33176 thanatophoric dysplasia San Diego type RGO:33176 ORDO:1860 RGO:33177 thanatophoric dysplasia type 1 RGO:33177 ORDO:93274 RGO:33178 thanatophoric dysplasia type 2 RGO:33178 RGO:33179 thrombocytopenia with distal limb defects RGO:33179 ORDO:77258 RGO:33181 trichorhinophalangeal dysplasia types 1/3 RGO:33181 RGO:33182 Weill-Marchesani syndrome dominant type RGO:33182 RGO:33183 Weill-Marchesani syndrome recessive type RGO:33183 DOID:0050463 RGO:33187 acampomelic campomelic dysplasia RGO:33187 RGO:33188 acrolaryngeal dysplasia RGO:33188 RGO:33191 dental malalignment RGO:33191 RGO:33192 Hapsburg jaw RGO:33192 drug effect drug therapy drugs SNOMEDCT:410942007 RGO:33195 drug RGO:33195 RGO:33197 anomalous pulmonary vessel RGO:33197 RGO:33198 fissure of azygos lobe RGO:33198 RGO:33199 fissure of hemiazygos lobe RGO:33199 RGO:33200 interlobar fissure RGO:33200 RGO:33201 accessory fissure RGO:33201 RADLEX:RID28513 SNOMEDCT:11689004 RGO:33202 linear atelectasis RGO:33202 SNOMEDCT:40779009 RGO:33203 plate-like atelectasis RGO:33203 RADLEX:RID880 SNOMEDCT:244247009 SNOMEDCT:64468002 RGO:33204 bronchial artery RGO:33204 RGO:33205 thin-walled cavity RGO:33205 RADLEX:RID46027 RGO:33206 bronchial wall thickening RGO:33206 SNOMEDCT:65615007 RGO:33210 Blastomyces dermatitidis RGO:33210 Emmonsia crescens SNOMEDCT:243505000 RGO:33212 Chrysosporium parvum RGO:33212 SNOMEDCT:23439005 RGO:33213 Coccidioides immitis RGO:33213 SNOMEDCT:67168003 RGO:33216 Cryptococcus neoformans RGO:33216 SNOMEDCT:56596006 RGO:33217 Histoplasma capsulatum RGO:33217 SNOMEDCT:61449004 RGO:33218 Paracoccidioides brasiliensis RGO:33218 SNOMEDCT:71825007 RGO:33219 Penicillium marneffei RGO:33219 SNOMEDCT:91088000 RGO:33222 Pseudoallescheria boydii RGO:33222 SNOMEDCT:32662000 RGO:33223 Sporothrix schenckii RGO:33223 SNOMEDCT:444877006 RGO:33224 Torulopsis glabrata RGO:33224 RGO:33226 parasitic lung disease RGO:33226 RGO:33227 bacterial lung disease RGO:33227 RGO:33229 rickettsial lung disease RGO:33229 SNOMEDCT:81559006 RGO:33231 Ancylostoma duodenale RGO:33231 SNOMEDCT:19061001 RGO:33232 Ascaris lumbricoides RGO:33232 SNOMEDCT:17894007 RGO:33233 Cysticercus cellulosae RGO:33233 RGO:33234 Dirofilaria infection RGO:33234 SNOMEDCT:4716008 RGO:33236 Entamoeba histolytica RGO:33236 SNOMEDCT:43905006 RGO:33237 Necator americanus RGO:33237 SNOMEDCT:40294009 RGO:33239 Paragonimus species RGO:33239 P. westermani SNOMEDCT:58412002 RGO:33240 Paragonimus westermani RGO:33240 SNOMEDCT:39091000 RGO:33242 Toxocara species RGO:33242 SNOMEDCT:11168007 RGO:33244 Schistosoma mansoni RGO:33244 SNOMEDCT:5249008 RGO:33245 Schistosoma japonicum RGO:33245 SNOMEDCT:36283001 RGO:33246 Toxocara cati RGO:33246 SNOMEDCT:4649006 RGO:33247 Toxoplasma gondii RGO:33247 T. canis SNOMEDCT:88857009 RGO:33248 Toxocara canis RGO:33248 RGO:33252 subperiosteal aneurysmal bone cyst RGO:33252 RGO:33253 chondrosarcoma arising from osteochondroma RGO:33253 SNOMEDCT:128421002 RGO:33254 ossifying fasciitis RGO:33254 RGO:33255 parosteal fasciitis RGO:33255 RGO:33257 subperiosteal ganglion RGO:33257 RGO:33258 subperiosteal osteoblastoma RGO:33258 RGO:33259 periosteal osteosarcoma RGO:33259 RGO:33260 parosteal hemangioma RGO:33260 RGO:33262 subperiosteal osteoid osteoma RGO:33262 reactivation TB SNOMEDCT:51014003 RGO:33264 reactivation tuberculosis RGO:33264 SNOMEDCT:90623003 RGO:33267 aluminum pneumoconiosis RGO:33267 RGO:33268 noxious inhalation RGO:33268 RGO:33271 acute schistosomiasis RGO:33271 RGO:33272 ECHO virus RGO:33272 SNOMEDCT:78981005 RGO:33273 Mycoplasma RGO:33273 DOID:11263 SNOMEDCT:16241000 RGO:33275 chlamydia RGO:33275 DOID:11262 ICD10CM:A70 SNOMEDCT:75116005 RGO:33276 psittacosis RGO:33276 TTN transient tachypnea of newborn RGO:33278 transient tachypnea of the newborn RGO:33278 RGO:33281 Hemophilus influenzae pneumonia RGO:33281 RGO:33282 atypical mycobacterial pneumonia RGO:33282 RGO:33283 exudative skin disorder RGO:33283 RGO:33284 acute pulmonary veno-occlusive disease RGO:33284 RGO:33287 hemorrhagic lung metastasis RGO:33287 RGO:33288 mineral oil aspiration RGO:33288 RGO:33289 silicoproteinosis RGO:33289 RGO:33290 foreign body in lung tissue RGO:33290 RGO:33291 untreated infection RGO:33291 RGO:33292 antibiotic-resistant pneumonia RGO:33292 RGO:33294 hypersensitivity bronchopulmonary aspergillosis RGO:33294 RGO:33296 right heart obstruction RGO:33296 RGO:33297 acute diffuse bronchiolitis RGO:33297 RGO:33299 chronic obstructive emphysema RGO:33299 RGO:33300 antitrypsin deficiency RGO:33300 RGO:33301 thermal bronchiolitis RGO:33301 SNOMEDCT:73342002 RGO:33303 tracheal obstruction RGO:33303 RGO:33304 tracheal narrowing RGO:33304 HP:0005945 RGO:33305 laryngeal obstruction RGO:33305 RGO:33306 laryngeal narrowing RGO:33306 RGO:33307 central pulmonary thromboembolism RGO:33307 RGO:33308 deep inspiration RGO:33308 RGO:33309 infantile diffuse bronchopneumonia RGO:33309 DOID:8469 SNOMEDCT:6142004 RGO:33310 influenza RGO:33310 RGO:33311 noxious vapors RGO:33311 RGO:33312 Asian panbronchiolitis RGO:33312 DOID:13278 ICD10CM:A02.22 SNOMEDCT:2523007 RGO:33314 salmonella pneumonia RGO:33314 SNOMEDCT:195889001 RGO:33315 Legionella pneumonia RGO:33315 RGO:33316 hematogenous metastases RGO:33316 RGO:33318 interstitial pulmonary edema with pulmonary venous hypertension RGO:33318 RGO:33319 lung trauma RGO:33319 SNOMEDCT:707376007 RGO:33320 pulmonary leiomyomatosis RGO:33320 RGO:33321 talc thromboembolism RGO:33321 RGO:33322 metallic mercury thromboembolism RGO:33322 ORDO:930 SNOMEDCT:715192004 RGO:33323 idiopathic achalasia RGO:33323 RGO:33325 necrotic adrenal metastasis RGO:33325 ICD10CM:P54.4 RGO:33326 neonatal adrenal hemorrhage RGO:33326 RGO:33327 post-traumatic hemorrhage RGO:33327 RGO:33330 paint fumes RGO:33330 SNOMEDCT:51765001 RGO:33332 carbon monoxide RGO:33332 RGO:33333 fluorocarbon inhalation RGO:33333 RGO:33334 hydrocarbon inhalation RGO:33334 ORDO:31827 RGO:33335 paraquat inhalation RGO:33335 RGO:33336 ammonium inhalation RGO:33336 SNOMEDCT:29276003 RGO:33337 chlorine gas RGO:33337 RGO:33338 hydrogen sulfide gas RGO:33338 RGO:33339 cadmium inhalation RGO:33339 RGO:33341 hematogenous lung metastases RGO:33341 RGO:33342 Chlamydia pneumonia RGO:33342 SNOMEDCT:110149000 RGO:33343 traumatic hemorrhage RGO:33343 SNOMEDCT:414916001 RGO:33344 adiposity RGO:33344 RGO:33345 collateral blood vessels RGO:33345 RGO:33346 internal mammary varices RGO:33346 RGO:33347 soft-tissue myeloma RGO:33347 RGO:33348 absent thymus in an infant RGO:33348 RGO:33349 infectious lymphadenitis RGO:33349 RGO:33350 idiopathic lymphadenitis RGO:33350 RGO:33351 undifferentiated lung carcinoma RGO:33351 SNOMEDCT:14189004 RGO:33352 rubeola RGO:33352 RGO:33353 aortic laceration RGO:33353 RGO:33354 mediastinal edema RGO:33354 RGO:33355 cylindical bronchiectasis RGO:33355 DOID:0050052 ICD10CM:A77.0 ORDO:83311 SNOMEDCT:186772009 RGO:33357 Rocky Mountain spotted fever RGO:33357 DOID:11100 ICD10CM:A78 ORDO:781 SNOMEDCT:186788009 RGO:33358 Q fever RGO:33358 RGO:33359 pulmonary thromboembolism with infarction RGO:33359 DOID:2154 HP:0002667 ORDO:654 RADLEX:RID4553 SNOMEDCT:25081006 SNOMEDCT:302849000 RGO:33360 nephroblastoma RGO:33360 SNOMEDCT:297156001 RGO:33361 axillary vein thrombosis RGO:33361 RGO:33362 adnexal mass RGO:33362 RGO:33363 malignant germ cell tumor RGO:33363 RGO:33364 simple ovarian cyst RGO:33364 HP:0000147 RGO:33365 polycystic ovary disease RGO:33365 RGO:33366 sex cord stromal tumor RGO:33366 RGO:33368 Krukenberg-type metastasis RGO:33368 SNOMEDCT:256896000 SNOMEDCT:266474003 RGO:33373 biliary calculus RGO:33373 SNOMEDCT:42463004 RGO:33375 Opisthorchis RGO:33375 RGO:33377 hemorrhagic renal cell carcinoma RGO:33377 RGO:33380 proteinaceous cyst RGO:33380 RGO:33381 inangiomyolipoma RGO:33381 SNOMEDCT:309089006 RGO:33383 prostate mass RGO:33383 RGO:33386 idiopathic mandibular periostitis RGO:33386 DOID:9768 SNOMEDCT:65340007 RGO:33390 cardiac aneurysm RGO:33390 RADLEX:RID34644 RGO:33391 diaphragmatic rupture RGO:33391 RGO:33392 diaphragmatic neoplasm RGO:33392 RGO:33393 herniation of liver RGO:33393 RGO:33394 esophagectomy with gastric pull-up RGO:33394 RGO:33395 esophagectomy with colon interposition RGO:33395 RGO:33396 juxtapericardial lymphadenopathy RGO:33396 RGO:33397 pleural adhesions RGO:33397 extralobar lung sequestration extralobar sequestration of lung ORDO:280811 RGO:33398 extralobar pulmonary sequestration RGO:33398 DOID:6201 HP:0100004 RGO:33399 pericardial mesothelioma RGO:33399 RGO:33400 squamous lung carcinoma RGO:33400 DOID:5563 RGO:33402 malignant teratoma RGO:33402 DOID:11934 HP:0012288 RADLEX:RID45697 RGO:33403 head and neck cancer RGO:33403 RGO:33404 reactive airways disease RGO:33404 RGO:33405 angioinvasive aspergillosis RGO:33405 DOID:12986 SNOMEDCT:30419000 RGO:33406 leukostasis RGO:33406 RGO:33407 leukemia cell lysis RGO:33407 SNOMEDCT:7895008 RGO:33410 drug toxicity RGO:33410 RGO:33411 poison toxicity RGO:33411 RGO:33412 Strongyloides pneumonia RGO:33412 RGO:33413 chronic pulmonary hemorrhage RGO:33413 RGO:33419 middle ear anomaly RGO:33419 RGO:33420 inner ear anomaly RGO:33420 HP:0001653 RADLEX:RID34748 SNOMEDCT:48724000 RGO:33421 mitral valve regurgitation RGO:33421 ORDO:95465 RGO:33422 cleft mitral valve RGO:33422 RGO:33424 rupture of posterior aortic sinus aneurysm into right atrium RGO:33424 ORDO:567 RGO:33425 chromosome 22q11.2 deletion RGO:33425 HP:0000777 RGO:33426 thymic hypoplasia RGO:33426 ORDO:83471 SNOMEDCT:91918005 RGO:33427 congenital thymic aplasia RGO:33427 RGO:33428 Strong syndrome RGO:33428 DOID:12583 SNOMEDCT:83092002 RGO:33429 Shprintzen syndrome RGO:33429 DOID:1363 RGO:33431 ethmoid sinus cancer RGO:33431 SNOMEDCT:363385007 RGO:33432 cancer of floor of mouth RGO:33432 DOID:1357 RGO:33433 maxillary sinus cancer RGO:33433 RGO:33434 nasopharyngeal cancer RGO:33434 DOID:0060119 RGO:33435 pharyngeal cancer RGO:33435 DOID:8649 RGO:33436 tongue cancer RGO:33436 RGO:33437 tonsillar cancer RGO:33437 T1-bright intracranial lesion RGO:33438 T1-hyperintense intracranial lesion RGO:33438 T2-bright intracranial lesion RGO:33439 T2-hyperintense intracranial lesion RGO:33439 T2-dark intracranial lesion RGO:33441 T2-hypointense intracranial lesion RGO:33441 T1-dark intracranial lesion RGO:33442 T1-hypointense intracranial lesion RGO:33442 RGO:33444 Actinomyces infection RGO:33444 RGO:33453 T1-isointense intracranial lesion RGO:33453 RGO:33454 T2-isointense intracranial lesion RGO:33454 RGO:33461 hypodense sellar lesion RGO:33461 RGO:33462 hypodense suprasellar lesion RGO:33462 RGO:33463 hyperdense sellar lesion RGO:33463 RGO:33464 hyperdense suprasellar lesion RGO:33464 RGO:33465 homogeneous T1-hypointense intracranial lesion RGO:33465 RGO:33466 homogeneous T2-hyperintense intracranial lesion RGO:33466 RGO:33467 heterogeneous T1-hypointense intracranial lesion RGO:33467 RGO:33468 heterogeneous T2-hyperintense intracranial lesion RGO:33468 RGO:33471 enhancing sellar lesion RGO:33471 RGO:33472 enhancing suprasellar lesion RGO:33472 RGO:33473 isodense sellar lesion RGO:33473 RGO:33474 isodense suprasellar lesion RGO:33474 RGO:33475 pseudocoarctation RGO:33475 RADLEX:RID5216 RGO:33476 fat deposition RGO:33476 HP:0001724 HP:0004942 RGO:33477 aortic dilatation RGO:33477 RGO:33478 post-treatment thymic rebound RGO:33478 RGO:33479 subacute cephalohematoma RGO:33479 RGO:33481 old infarction RGO:33481 RGO:33482 densely calcified meningioma RGO:33482 RGO:33483 supraclinoid carotid aneurysm RGO:33483 RGO:33484 basilar tip aneurysm RGO:33484 RGO:33485 cavernous carotid aneurysm RGO:33485 RGO:33486 metastatic breast carcinoma RGO:33486 RGO:33487 benign external hydrocephalus RGO:33487 RGO:33494 partial supraspinatus tendon tear RGO:33494 HP:0025230 RADLEX:RID3649 SNOMEDCT:34840004 RGO:33495 tendonitis RGO:33495 RGO:33496 supraspinatus tendon tear RGO:33496 RGO:33497 tumefactive sludge RGO:33497 RGO:33498 pulmonary segmental consolidation RGO:33498 RGO:33499 pulmonary lobar consolidation RGO:33499 RGO:33500 compensatory distention of adjacent lobe RGO:33500 RGO:33501 endobronchial obstruction RGO:33501 RGO:33502 extrabronchial compression RGO:33502 RGO:33503 extrabronchial obstruction RGO:33503 RGO:33504 pulmonary artery compression RGO:33504 RGO:33506 unilateral hyperlucency of chest RGO:33506 RGO:33511 metastasis to central canal RGO:33511 RADLEX:RID5123 RGO:33512 tendonosis RGO:33512 RGO:33513 tendon tear RGO:33513 SNOMEDCT:235972007 RGO:33515 pancreatic duct stricture RGO:33515 sludge SNOMEDCT:27123005 RGO:33516 biliary sludge RGO:33516 SNOMEDCT:235974008 RGO:33517 pancreatic duct calculus RGO:33517 RGO:33519 confluent fibrosis RGO:33519 RGO:33520 post-radiation hepatitis RGO:33520 RADLEX:RID3879 RGO:33521 regenerative nodule RGO:33521 RADLEX:RID3880 SNOMEDCT:448149008 RGO:33522 dysplastic nodule RGO:33522 RGO:33523 mucinous adenocarcinoma metastasis RGO:33523 RGO:33524 colon cancer metastasis RGO:33524 RGO:33525 pancreatic cancer metastasis RGO:33525 RGO:33526 intratumoral hematoma RGO:33526 RGO:33528 acute posttraumatic hematoma RGO:33528 RGO:33529 acute intratumoral hemorrhage RGO:33529 RGO:33530 focal iron deposition RGO:33530 RGO:33531 siderotic dysplastic nodule RGO:33531 RGO:33532 siderotic regenerative nodule RGO:33532 RGO:33533 treated neoplasm RGO:33533 RGO:33534 postoperative CSF leak RGO:33534 RGO:33535 peribiliary cysts RGO:33535 RGO:33536 metastasis to porta hepatis RGO:33536 RGO:33537 vascular resuscitation RGO:33537 RGO:33539 uterine sarcoma with hemorrhage RGO:33539 SNOMEDCT:70514001 RGO:33540 uterine contraction RGO:33540 RGO:33543 uterine sarcoma with necrosis RGO:33543 RADLEX:RID4531 RGO:33545 mixed müllerian tumor RGO:33545 RGO:33547 obstructed cervix RGO:33547 RGO:33548 cervical carcinoma RGO:33548 RGO:33549 obstructed horn in uterine didelphys RGO:33549 RGO:33550 obstructed endometrium RGO:33550 RGO:33551 endometrial carcinoma with hemorrhage RGO:33551 RGO:33552 chronic hematometra RGO:33552 RGO:33555 osteomyelitis with adjacent cellulitis RGO:33555 RGO:33556 fracture fragment RGO:33556 RADLEX:RID46073 SNOMEDCT:277762005 RGO:33557 lumbar puncture RGO:33557 RGO:33558 myelophthisic marrow replacement RGO:33558 RGO:33559 diffuse marrow replacement by tumor RGO:33559 RGO:33560 diffuse metastatic disease RGO:33560 RGO:33562 acute cephalohematoma RGO:33562 RGO:33563 chronic cephalohematoma RGO:33563 DOID:4723 HP:0012641 RADLEX:RID4958 SNOMEDCT:433691000124104 RGO:33564 intracranial hypotension RGO:33564 RGO:33565 dural tail meningioma RGO:33565 RGO:33566 dural metastasis RGO:33566 RGO:33567 allergic angitis RGO:33567 DOID:670 SNOMEDCT:84758004 RGO:33568 amphetamine abuse RGO:33568 RGO:33569 serum sickness vasculitis RGO:33569 RGO:33570 serum sickness-like vasculitis RGO:33570 RGO:33571 idiopathic cerebral vasculitis RGO:33571 RGO:33573 dense calcification RGO:33573 RGO:33574 enlarged medullary vein RGO:33574 RGO:33575 metallic artifact RGO:33575 RADLEX:RID5608 SNOMEDCT:468403003 RGO:33576 aneurysm clip RGO:33576 RGO:33577 traumatic bone fragment RGO:33577 RGO:33578 collateral vessels RGO:33578 RGO:33579 posttraumatic arachnoid tear RGO:33579 RGO:33580 benign subdural effusion RGO:33580 SNOMEDCT:276674008 RGO:33581 neonatal meningitis RGO:33581 RGO:33582 normal CSF flow RGO:33582 RGO:33583 hyperdynamic CSF flow RGO:33583 RGO:33584 shunt-responsive normal pressure hydrocephalus RGO:33584 RGO:33585 invasive carcinoma of cervix RGO:33585 RGO:33586 invasive carcinoma of endometrium RGO:33586 RGO:33587 leiomyoma with degeneration RGO:33587 RGO:33588 sarcoma with necrosis RGO:33588 RGO:33589 leiomyosarcoma with necrosis RGO:33589 RGO:33590 leiomyoma with edema RGO:33590 RGO:33591 basilar racemose form of cysticercosis RGO:33591 RGO:33593 upper cervical neurofibroma extending through foramen magnum RGO:33593 RGO:33594 cranial nerve schwannoma RGO:33594 cavum velum interpositum RGO:33595 cavum veli interpositi RGO:33595 black epidermoid RGO:33600 solid cholesterol epidermoid RGO:33600 RGO:33602 postictal hyperemia RGO:33602 RGO:33603 subjacent acute cerebral infarction RGO:33603 RGO:33604 leptomeningeal collaterals RGO:33604 RGO:33605 subacute cerebral infarction RGO:33605 RGO:33606 benign meningeal fibrosis RGO:33606 SNOMEDCT:255127006 RGO:33607 local tumor spread RGO:33607 RGO:33608 calcified meningioma RGO:33608 RGO:33609 ossification of falx cerebri RGO:33609 RGO:33610 diffuse cerebral edema RGO:33610 RGO:33611 chronic multiple sclerosis RGO:33611 RGO:33612 postinfectious RGO:33612 RGO:33614 global cerebral ischemia RGO:33614 RGO:33615 intraventricular cysticercosis RGO:33615 RGO:33616 tumor at foramen of Monro RGO:33616 RGO:33617 tumor at aqueduct RGO:33617 RGO:33618 tumor at fourth ventricle RGO:33618 RGO:33619 tumor at cerebellopontine angle RGO:33619 DOID:13948 SNOMEDCT:399072004 RGO:33627 bladder neck obstruction RGO:33627 RGO:33628 postsurgical bladder neck stricture RGO:33628 RGO:33629 posttraumatic bladder neck stricture RGO:33629 HP:0030711 RGO:33630 hydrocolpos RGO:33630 SNOMEDCT:90053006 RGO:33631 hematocolpometra RGO:33631 SNOMEDCT:7063008 RGO:33632 necrotizing pneumonia RGO:33632 SNOMEDCT:125571002 RGO:33633 lobectomy RGO:33633 SNOMEDCT:86743009 RGO:33634 local resection RGO:33634 SNOMEDCT:29068008 RGO:33635 therapeutic pneumothorax RGO:33635 HP:0002108 SNOMEDCT:80423007 RGO:33636 spontaneous pneumothorax RGO:33636 RGO:33637 idiopathic subarachnoid hemorrhage RGO:33637 chromosome 2(del 2q) syndrom RGO:33638 chromosome 2q deletion syndrome RGO:33638 RGO:33641 extravasated contrast medium RGO:33641 SNOMEDCT:274732007 RGO:33642 urinary extravasation RGO:33642 SNOMEDCT:197808006 RGO:33643 idiopathic retroperitoneal fibrosis RGO:33643 HP:0008676 ICD10CM:Q62.2 SNOMEDCT:718485003 RGO:33647 congenital megaureter RGO:33647 RGO:33648 urinary tract infection with stricture RGO:33648 RGO:33649 urinary flow increase RGO:33649 SNOMEDCT:95575002 RGO:33650 ureteropelvic obstruction RGO:33650 ORDO:1398 RGO:33658 isolated cerebellar hypoplasia RGO:33658 ectopia lentis syndrome familial ectopia lentis HP:0001083 ORDO:1885 RGO:33679 isolated ectopia lentis RGO:33679 ORDO:1909 SNOMEDCT:715430001 RGO:33682 indomethacin embryofetopathy RGO:33682 ID MR impaired intelligence intellectual deficiency intellectual disability intellectual impairment mental retardation RGO:33684 intellectual deficit RGO:33684 HP:0001199 RGO:33688 triphalangeal thumbs RGO:33688 RGO:33689 maxillary diastema RGO:33689 Norman disease PCH1 ORDO:2254 RGO:33690 pontocerebellar hypoplasia type 1 RGO:33690 IFAP syndrome ichthyosis - atrichia - photophobia ichthyosis follicularis - atrichia - photophobia syndrome ichthyosis-alopecia-photophobia syndrome RGO:33694 ichthyosis follicularis - alopecia - photophobia RGO:33694 ORDO:2343 RGO:33704 isolated cloverleaf skull syndrome RGO:33704 HP:0000506 SNOMEDCT:246803005 RGO:33710 telecanthus RGO:33710 RGO:33713 congenital pulmonary lymphangiectasis RGO:33713 ORDO:2524 SNOMEDCT:715463008 RGO:33721 pontocerebellar hypoplasia type 2 RGO:33721 DOID:0050788 HP:0100264 ORDO:3250 RGO:33765 proximal symphalangism RGO:33765 ORDO:3188 RGO:33768 congenital pulmonary vein atresia or stenosis RGO:33768 ORDO:3202 SNOMEDCT:715526002 RGO:33781 dehydrated hereditary stomatocytosis RGO:33781 ORDO:3203 RGO:33782 overhydrated hereditary stomatocytosis RGO:33782 ORDO:3366 RGO:33784 isolated trigonocephaly RGO:33784 HP:0011627 ORDO:3400 RGO:33786 aorto-ventricular tunnel RGO:33786 ORDO:33110 RGO:33788 autosomal agammaglobulinemia RGO:33788 HP:0030799 ORDO:35093 RGO:33789 isolated scaphocephaly RGO:33789 HP:0001357 ORDO:35098 RGO:33790 isolated plagiocephaly RGO:33790 ORDO:35099 RGO:33791 isolated brachycephaly RGO:33791 ORDO:50811 RGO:33796 lipodystrophy - intellectual deficit - deafness RGO:33796 HP:0000263 ORDO:63440 RGO:33801 isolated oxycephaly RGO:33801 DOID:0110002 ORDO:67046 SNOMEDCT:237951008 RGO:33819 3-methylglutaconic aciduria type 1 RGO:33819 Costeff optic atrophy syndrome Costeff syndrome MGA3 optic atrophy plus syndrome DOID:0110004 ORDO:67047 SNOMEDCT:297232009 RGO:33820 3-methylglutaconic aciduria type 3 RGO:33820 DOID:0110006 ORDO:67048 SNOMEDCT:297233004 RGO:33825 3-methylglutaconic aciduria type 4 RGO:33825 ORDO:69723 SNOMEDCT:415764005 RGO:33827 tyrosinemia type 3 RGO:33827 ORDO:71269 RGO:33829 benign exophthalmos syndrome RGO:33829 XLSA DOID:0060063 ORDO:75563 SNOMEDCT:62677000 RGO:33833 X-linked sideroblastic anemia RGO:33833 SGBS2 lethal variant of Simpson-Golabi-Behmel syndrome ORDO:79022 RGO:33835 Simpson-Golabi-Behmel syndrome type 2 RGO:33835 BSEP deficiency PFIC2 ORDO:79304 RGO:33864 progressive familial intrahepatic cholestasis type 2 RGO:33864 PFIC3 ORDO:79305 RGO:33867 progressive familial intrahepatic cholestasis type 3 RGO:33867 SNOMEDCT:17302008 RGO:33880 cerebellar sarcoma RGO:33880 DOID:231 ICD10CM:G12.2 SNOMEDCT:37340000 RGO:33884 motor neuron disease RGO:33884 RGO:33885 motor neuropathy RGO:33885 RGO:33886 arteriovenous malformation of spinal cord RGO:33886 Meige lymphedema hereditary lymphedema type 2 ORDO:90186 RGO:33887 Meige disease RGO:33887 ORDO:91397 RGO:33895 isolated ankyloblepharon filiforme adnatum RGO:33895 HP:0000122 ORDO:93100 RGO:33897 unilateral renal agenesis RGO:33897 HP:0010736 ORDO:93277 SNOMEDCT:89859004 RGO:33899 monostotic fibrous dysplasia RGO:33899 ORDO:95449 RGO:33906 congenital aortic valve insufficiency RGO:33906 HP:0000054 ORDO:95707 RGO:33907 isolated micropenis RGO:33907 RGO:33909 tetrasomy syndrome RGO:33909 DOID:0060272 ORDO:97249 RGO:33910 pontocerebellar hypoplasia type 3 RGO:33910 bilateral multicystic dysplastic kidneys multicystic dysplastic kidneys ORDO:97364 RGO:33911 bilateral multicystic renal dysplasia RGO:33911 ORDO:99789 RGO:33916 dentin dysplasia type 1 RGO:33916 ORDO:99791 RGO:33917 dentin dysplasia type 2 RGO:33917 RGO:33927 submucosal cleft palate RGO:33927 alopecia - progressive neurological defect - endocrinopathy ORDO:157954 RGO:33928 ANE syndrome RGO:33928 progressive neurological deterioration RGO:33930 progressive neurological defect RGO:33930 ORDO:166282 SNOMEDCT:233913007 RGO:33936 familial sick sinus syndrome RGO:33936 ORDO:168552 RGO:33937 spondylometaphyseal dysplasia - bowed forearms - facial dysmorphism RGO:33937 RGO:33938 bowed forearm RGO:33938 HP:0100771 RGO:33939 intestinal hypoperistalsis RGO:33939 ORDO:168624 RGO:33941 familial scaphocephaly syndrome McGillivray type RGO:33941 ORDO:171703 RGO:33942 microcephaly - polymicrogyria - corpus callosum agenesis RGO:33942 ORDO:171836 RGO:33943 amelogenesis imperfecta - gingival hyperplasia syndrome RGO:33943 HP:0000212 RGO:33944 gingival hyperplasia RGO:33944 Berant syndrome ORDO:171839 RGO:33945 craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis RGO:33945 ORDO:171844 RGO:33946 blindness - scoliosis - arachnodactyly RGO:33946 ORDO:171848 RGO:33947 polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract RGO:33947 DOID:1389 HP:0001271 ICD10CM:A69.22 SNOMEDCT:42345000 RGO:33948 polyneuropathy RGO:33948 ORDO:171860 RGO:33949 intellectual deficit - cataracts - kyphosis RGO:33949 ORDO:178377 RGO:33951 osteosclerosis - developmental delay - craniosynostosis RGO:33951 RGO:33954 pneumomed RGO:33954 Caffey tibial spine osteonecrosis RGO:33960 osteonecrosis of the intercondylar spines of the tibia RGO:33960 elevated cortisol DOID:3947 HP:0003118 SNOMEDCT:47270006 RGO:33962 hypercortisolism RGO:33962 secondary hypertrophic osteoarthropathy RGO:33999 pulmonary hypertrophic osteoarthropathy RGO:33999 SNOMEDCT:59277005 RGO:34002 phycomycosis RGO:34002 DOID:0050278 SNOMEDCT:4921002 RGO:34003 basidiobolomycosis RGO:34003 ORDO:231013 RGO:34011 congenital trigeminal anesthesia RGO:34011 ORDO:250923 RGO:34012 isolated aniridia RGO:34012 ICD10CM:L26 SNOMEDCT:399992009 RGO:34016 exfoliative dermatitis RGO:34016 ORDO:309854 RGO:34025 cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome RGO:34025 DOID:543 HP:0001332 ICD10CM:G24 SNOMEDCT:15802004 RGO:34026 dystonia RGO:34026 RGO:34027 hypermanganesemia RGO:34027 ORDO:314555 RGO:34029 craniofacial dysplasia - osteopenia syndrome RGO:34029 RGO:34030 Hamamy syndrome RGO:34030 RGO:34031 craniofacial dysplasia RGO:34031 ORDO:314575 RGO:34032 intellectual deficit - hypotonia - brachycephaly - pyloric stenosis - cryptorchidism syndrome RGO:34032 hypertrichosis - short stature - facial dysmorphism - developmental delay syndrome ORDO:319182 RGO:34033 Wiedemann-Steiner syndrome RGO:34033 Carney complex variant ORDO:319340 RGO:34035 Carney complex - trismus - pseudocamptodactyly syndrome RGO:34035 RGO:34036 pseudocamptodactyly RGO:34036 ORDO:324410 RGO:34038 X-linked intellectual deficit - cardiomegaly - congestive heart failure RGO:34038 ORDO:324416 RGO:34039 muscular hypertrophy - hepatomegaly - polyhydramnios RGO:34039 ORDO:324540 RGO:34040 aphonia - deafness - retinal dystrophy - bifid halluces - intellectual deficit RGO:34040 ICD10CM:R49.1 SNOMEDCT:441913003 RGO:34041 aphonia RGO:34041 DOID:8501 HP:0000556 SNOMEDCT:314407005 RGO:34042 retinal dystrophy RGO:34042 RGO:34043 bifid hallux RGO:34043 ORDO:329224 RGO:34044 intellectual deficit - craniofacial dysmorphism - cryptorchidism RGO:34044 RGO:34045 craniofacial dysmorphism RGO:34045 ORDO:329332 RGO:34046 microcephaly - cerebellar hypoplasia - cardiac conduction defect syndrome RGO:34046 spondyloepiphyseal dysplasia - retinal dystrophy - immunodeficiency ORDO:353298 RGO:34047 Roifman syndrome RGO:34047 HP:0002721 SNOMEDCT:234532001 RGO:34049 immunodeficiency RGO:34049 DOID:0060407 SNOMEDCT:270889005 RGO:34050 18q- syndrome RGO:34050 ORDO:847 RGO:34052 alpha thalassemia - X-linked intellectual deficit syndrome RGO:34052 ORDO:929 RGO:34053 achalasia - microcephaly RGO:34053 ORDO:988 RGO:34054 absent tibia - polydactyly RGO:34054 ORDO:990 RGO:34055 agnathia - holoprosencephaly - situs inversus RGO:34055 ORDO:1005 RGO:34056 alopecia - contractures - dwarfism - intellectual deficit RGO:34056 ORDO:1008 RGO:34057 alopecia - epilepsy - pyorrhea - intellectual deficit RGO:34057 ORDO:1014 RGO:34058 alopecia - intellectual deficit - hypergonadotropic hypogonadism RGO:34058 DOID:5426 HP:0000815 SNOMEDCT:370999003 RGO:34059 hypergonadotropic hypogonadism RGO:34059 ORDO:1018 RGO:34060 X-linked diffuse leiomyomatosis - Alport syndrome RGO:34060 HP:0006756 RGO:34061 diffuse leiomyomatosis RGO:34061 ORDO:1021 RGO:34062 amaurosis - hypertrichosis RGO:34062 SNOMEDCT:70449006 RGO:34063 amaurosis RGO:34063 ORDO:1046 RGO:34064 lethal hemolytic anemia - genital anomalies RGO:34064 RGO:34065 lethal hemolytic anemia RGO:34065 ORDO:1051 RGO:34066 corneal anesthesia - deafness - intellectual deficit RGO:34066 SNOMEDCT:373423002 RGO:34067 corneal anesthesia RGO:34067 ORDO:1057 RGO:34068 intracranial aneurysms - multiple congenital anomalies RGO:34068 cerebral aneurysm DOID:10941 HP:0004944 SNOMEDCT:128609009 RGO:34069 intracranial aneurysm RGO:34069 SNOMEDCT:400038003 RGO:34070 multiple congenital anomalies RGO:34070 ORDO:1064 RGO:34071 aniridia - renal agenesis - psychomotor retardation RGO:34071 ORDO:1065 RGO:34072 aniridia - cerebellar ataxia - intellectual deficit RGO:34072 ORDO:1067 RGO:34073 aniridia - ptosis - intellectual deficit - familial obesity RGO:34073 DOID:0060260 HP:0000508 RADLEX:RID4795 SNOMEDCT:11934000 SNOMEDCT:29696001 RGO:34074 ptosis RGO:34074 SNOMEDCT:290439001 RGO:34075 familial obesity RGO:34075 ORDO:1069 RGO:34076 aniridia - absent patella RGO:34076 ORDO:1074 RGO:34077 ankyloblepharon filiforme - imperforate anus RGO:34077 RGO:34078 ankyloblepharon filiforme RGO:34078 ORDO:1078 RGO:34079 thumb stiffness - brachydactyly - intellectual deficit RGO:34079 RGO:34080 thumb stiffness RGO:34080 ORDO:1088 RGO:34081 short stature - heart defect - craniofacial anomalies RGO:34081 DOID:1682 HP:0030680 RGO:34082 heart defect RGO:34082 ORDO:1094 RGO:34083 anonychia - microcephaly RGO:34083 ORDO:1101 RGO:34084 anophthalmia - megalocornea - cardiopathy - skeletal anomalies RGO:34084 SNOMEDCT:56265001 RGO:34085 cardiopathy RGO:34085 HP:0000924 RGO:34086 skeletal anomalies RGO:34086 ORDO:1110 RGO:34087 aortic arch anomaly - peculiar facies - intellectual deficit RGO:34087 ORDO:1113 RGO:34088 aphalangy - syndactyly - microcephaly RGO:34088 ORDO:1116 RGO:34089 aplasia cutis congenita - intestinal lymphangiectasia RGO:34089 ORDO:1117 RGO:34090 aplasia cutis - myopia RGO:34090 ORDO:1120 RGO:34091 lung agenesis - heart defect - thumb anomalies RGO:34091 RGO:34092 lung agenesis RGO:34092 RGO:34093 thumb anomaly RGO:34093 ORDO:1122 RGO:34094 ulnar hypoplasia - split foot RGO:34094 HP:0001839 ICD10CM:Q72.7 SNOMEDCT:205358006 RGO:34095 split foot RGO:34095 ORDO:1123 RGO:34096 caudal appendage - deafness RGO:34096 ORDO:1129 RGO:34097 arachnodactyly - abnormal ossification - intellectual deficit RGO:34097 SNOMEDCT:36123008 RGO:34098 abnormal ossification RGO:34098 ORDO:1130 RGO:34099 arachnodactyly - intellectual deficit - dysmorphism RGO:34099 ORDO:1135 RGO:34100 arrhinia - choanal atresia - microphthalmia RGO:34100 HP:0009927 SNOMEDCT:111317000 RGO:34101 arrhinia RGO:34101 ORDO:1139 RGO:34102 arthrogryposis - epileptic seizures - migrational brain disorder RGO:34102 SNOMEDCT:84757009 RGO:34103 epileptic seizures RGO:34103 HP:0002269 RGO:34104 migrational brain disorder RGO:34104 ORDO:1144 RGO:34105 arthrogryposis-like hand anomaly - sensorineural deafness RGO:34105 HP:0005612 RGO:34106 arthrogryposis-like hand anomaly RGO:34106 ORDO:1150 RGO:34107 arthrogryposis multiplex congenita - whistling face RGO:34107 ICD10CM:Q87.0 RGO:34108 whistling face RGO:34108 ORDO:1167 RGO:34109 facial asymmetry - temporal seizures RGO:34109 RGO:34110 temporal seizures RGO:34110 ORDO:1168 RGO:34111 ataxia - oculomotor apraxia type 1 RGO:34111 HP:0000657 SNOMEDCT:193662007 RGO:34112 oculomotor apraxia RGO:34112 ORDO:1173 RGO:34113 cerebellar ataxia - hypogonadism RGO:34113 ORDO:1174 RGO:34114 cerebellar ataxia - ectodermal dysplasia RGO:34114 ORDO:1178 RGO:34115 ataxia - tapetoretinal degeneration RGO:34115 HP:0000547 RGO:34116 tapetoretinal degeneration RGO:34116 ORDO:1180 RGO:34117 ataxia - hypogonadism - choroidal dystrophy RGO:34117 HP:0007712 SNOMEDCT:312918002 RGO:34118 choroidal dystrophy RGO:34118 ORDO:1184 RGO:34119 ataxia - photosensitivity - short stature RGO:34119 ORDO:1185 RGO:34120 spinocerebellar ataxia - dysmorphism RGO:34120 ORDO:1192 RGO:34121 atherosclerosis - deafness - diabetes - epilepsy - nephropathy RGO:34121 ORDO:1200 RGO:34122 choanal atresia - deafness - cardiac defects - dysmorphism RGO:34122 RGO:34123 cardiac defects RGO:34123 ORDO:1211 RGO:34124 atrichia - mental and growth delay RGO:34124 RGO:34125 mental and growth delay RGO:34125 ORDO:1217 RGO:34126 spinal atrophy - ophthalmoplegia - pyramidal syndrome RGO:34126 RGO:34127 spinal atrophy RGO:34127 DOID:539 HP:0000602 SNOMEDCT:16110005 RGO:34128 ophthalmoplegia RGO:34128 RGO:34129 pyramidal syndrome RGO:34129 ORDO:1236 RGO:34130 intellectual deficit - athetosis - microphthalmia RGO:34130 HP:0002305 SNOMEDCT:44913001 RGO:34131 athetosis RGO:34131 ORDO:1246 RGO:34132 brachydactyly - nystagmus - cerebellar ataxia RGO:34132 ORDO:1256 RGO:34133 blepharophimosis - radioulnar synostosis RGO:34133 ORDO:1258 RGO:34134 blepharoptosis - cleft palate - ectrodactyly - dental anomalies RGO:34134 DOID:0060260 HP:0000508 SNOMEDCT:11934000 RGO:34135 blepharoptosis RGO:34135 ORDO:1259 RGO:34136 blepharoptosis - myopia - ectopia lentis RGO:34136 ORDO:1277 RGO:34137 brachydactyly - mesomelia - intellectual deficit - heart defects RGO:34137 HP:0003027 RGO:34138 mesomelia RGO:34138 RGO:34139 heart defects RGO:34139 ORDO:1278 RGO:34140 brachydactyly - preaxial hallux varus RGO:34140 RGO:34141 preaxial hallux varus RGO:34141 ORDO:1295 RGO:34142 brachytelephalangy - dysmorphism - Kallmann syndrome RGO:34142 HP:0006118 RGO:34143 brachytelephalangy RGO:34143 ORDO:1307 RGO:34144 distal limb deficiencies - micrognathia syndrome RGO:34144 RGO:34145 distal limb deficiency RGO:34145 ORDO:1321 RGO:34146 camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia RGO:34146 RGO:34147 fibrous tissue hyperplasia RGO:34147 ORDO:1323 RGO:34148 camptodactyly - joint contractures - facial skeletal defects RGO:34148 HP:0001371 RGO:34149 joint contractures RGO:34149 RGO:34150 facial skeletal defects RGO:34150 ORDO:1325 RGO:34151 camptodactyly - taurinuria RGO:34151 RGO:34152 taurinuria RGO:34152 ORDO:1338 RGO:34153 heart defect - tongue hamartoma - polysyndactyly RGO:34153 ORDO:1345 RGO:34154 cardiomyopathy - cataract - hip spine disease RGO:34154 RGO:34155 hip spine disease RGO:34155 ORDO:1352 RGO:34156 atrioventricular defect - blepharophimosis - radial defects RGO:34156 RGO:34157 atrioventricular defect RGO:34157 ORDO:1354 RGO:34158 heart defects - limb shortening RGO:34158 HP:0009826 RGO:34159 limb shortening RGO:34159 ORDO:1355 RGO:34160 heart defect - round face - congenital developmental delay RGO:34160 HP:0000311 RGO:34161 round face RGO:34161 ORDO:1368 RGO:34162 cataract - ataxia - deafness RGO:34162 ORDO:1369 RGO:34163 congenital cataract - hypertrophic cardiomyopathy - mitochondrial myopathy RGO:34163 HP:0000519 ICD10CM:Q12.0 SNOMEDCT:609587005 SNOMEDCT:79410001 RGO:34164 congenital cataract RGO:34164 DOID:11984 HP:0001639 RADLEX:RID3251 SNOMEDCT:233873004 RGO:34165 hypertrophic cardiomyopathy RGO:34165 cataract - hypertrichosis - mental retardation ORDO:1375 RGO:34166 cataract - hypertrichosis - intellectual deficit RGO:34166 ORDO:1376 RGO:34167 congenital cataract - ichthyosis RGO:34167 ORDO:1380 RGO:34168 cataract - nephropathy - encephalopathy RGO:34168 ORDO:1381 RGO:34169 cataract - intellectual deficit - anal atresia - urinary defects RGO:34169 RGO:34170 urinary defect RGO:34170 ORDO:1383 RGO:34171 cataract - deafness - hypogonadism RGO:34171 ORDO:1387 RGO:34172 cataract - intellectual deficit - hypogonadism RGO:34172 ORDO:1389 RGO:34173 cortical blindness - intellectual deficit - polydactyly RGO:34173 DOID:11831 HP:0100704 ICD10CM:H47.61 SNOMEDCT:68574006 RGO:34174 cortical blindness RGO:34174 ORDO:1390 RGO:34175 night blindness - skeletal anomalies - dysmorphism RGO:34175 DOID:8499 HP:0000662 ICD10CM:H53.6 SNOMEDCT:65194006 RGO:34176 night blindness RGO:34176 RGO:34177 skeletal anomaly RGO:34177 ORDO:1397 RGO:34178 cerebellum agenesis - hydrocephaly RGO:34178 HP:0012642 RGO:34179 cerebellar agenesis RGO:34179 ORDO:1408 RGO:34180 hair defect - photosensitivity - intellectual deficit RGO:34180 ORDO:1409 RGO:34181 woolly hair - hypotrichosis - everted lower lip - outstanding ears RGO:34181 HP:0002224 SNOMEDCT:52564001 RGO:34182 woolly hair RGO:34182 HP:0000232 RGO:34183 everted lower lip RGO:34183 RGO:34184 outstanding ears RGO:34184 ORDO:1414 RGO:34185 cholestasis - lymphedema RGO:34185 ORDO:1415 RGO:34186 cholestasis - pigmentary retinopathy - cleft palate RGO:34186 ORDO:1433 RGO:34187 choroidal atrophy - alopecia RGO:34187 SNOMEDCT:247200005 RGO:34188 choroidal atrophy RGO:34188 ORDO:1434 RGO:34189 choroideremia - hypopituitarism RGO:34189 DOID:9821 HP:0001139 ICD10CM:H31.21 SNOMEDCT:75241009 RGO:34190 choroideremia RGO:34190 ORDO:1435 RGO:34191 choroideremia - deafness - obesity RGO:34191 ORDO:1471 RGO:34192 coloboma of macula - brachydactyly type B RGO:34192 DOID:12270 RGO:34193 coloboma of macula RGO:34193 ORDO:1473 RGO:34194 uveal coloboma - cleft lip and palate - intellectual deficit RGO:34194 RGO:34195 uveal coloboma RGO:34195 RGO:34196 cleft lip and palate RGO:34196 ORDO:1479 RGO:34197 atrial septal defect - atrioventricular conduction defects RGO:34197 RGO:34198 atrioventricular conduction defect RGO:34198 ORDO:1484 RGO:34199 contractures - ectodermal dysplasia - cleft lip/palate RGO:34199 ORDO:1485 RGO:34200 arthrogryposis-hyperkeratosis lethal form RGO:34200 ORDO:1490 RGO:34202 corneal dystrophy - perceptive deafness RGO:34202 DOID:10003 SNOMEDCT:60700002 RGO:34203 perceptive deafness RGO:34203 ORDO:1492 RGO:34204 corpus callosum agenesis - double urinary collecting system RGO:34204 RGO:34205 double urinary collecting system RGO:34205 ORDO:1495 RGO:34206 intellectual deficit - hypoplastic corpus callosum - preauricular tag RGO:34206 ORDO:1496 RGO:34207 corpus callosum agenesis - neuronopathy RGO:34207 RGO:34208 neuronopathy RGO:34208 ORDO:1506 RGO:34209 thin ribs - tubular bones - dysmorphism RGO:34209 RGO:34210 tubular bones RGO:34210 ORDO:1514 RGO:34211 craniodigital syndrome - intellectual deficit RGO:34211 RGO:34212 craniodigital syndrome RGO:34212 ORDO:1521 RGO:34213 craniofrontonasal dysplasia - Poland anomaly RGO:34213 ORDO:1526 RGO:34214 craniosynostosis - synostoses - hypertensive nephropathy RGO:34214 RGO:34215 synostoses RGO:34215 ORDO:1530 RGO:34216 craniosynostosis - cataract RGO:34216 ORDO:1533 RGO:34217 craniosynostosis - fibular aplasia RGO:34217 ORDO:1535 RGO:34218 craniosynostosis - dysmorphism - brachydactyly RGO:34218 ORDO:1538 RGO:34219 craniosynostosis - Dandy-Walker - hydrocephalus RGO:34219 ORDO:1548 RGO:34220 cryptorchidism - arachnodactyly - intellectual deficit RGO:34220 ORDO:1562 RGO:34221 dacryocystitis - osteopoikilosis RGO:34221 ORDO:1564 RGO:34222 dandy Walker - facial hemangioma RGO:34222 RGO:34223 Dandy Walker malformation RGO:34223 HP:0000329 RGO:34224 facial hemangioma RGO:34224 ORDO:1566 RGO:34225 Dandy-Walker malformation - postaxial polydactyly RGO:34225 ORDO:1568 RGO:34226 X-linked intellectual deficit - Dandy-Walker malformation - basal ganglia disease - seizures RGO:34226 DOID:679 HP:0002134 RGO:34227 basal ganglia disease RGO:34227 ORDO:1574 RGO:34228 retinal degeneration - nanophthalmos - glaucoma RGO:34228 DOID:10629 HP:0000568 SNOMEDCT:204108000 RGO:34229 nanophthalmos RGO:34229 ORDO:1654 RGO:34230 natal teeth - intestinal pseudo-obstruction - patent ductus RGO:34230 RGO:34231 patent ductus RGO:34231 ORDO:1655 RGO:34232 mullerian derivatives - lymphangiectasia - polydactyly RGO:34232 RGO:34233 mullerian derivatives RGO:34233 ORDO:1658 RGO:34234 absence of fingerprints - congenital milia RGO:34234 RGO:34235 absence of fingerprints RGO:34235 RGO:34236 congenital milia RGO:34236 ORDO:1682 RGO:34237 arterial dissection - lentiginosis RGO:34237 SNOMEDCT:402624000 RGO:34238 lentiginosis RGO:34238 ORDO:1683 RGO:34239 distichiasis - congenital heart defects - peripheral vascular anomalies RGO:34239 HP:0009743 SNOMEDCT:95339000 RGO:34240 distichiasis RGO:34240 DOID:1682 HP:0001627 HP:0002564 RGO:34241 congenital heart defect RGO:34241 RGO:34242 peripheral vascular anomaly RGO:34242 ORDO:1765 RGO:34243 dyschondrosteosis - nephritis RGO:34243 ORDO:1770 RGO:34244 gonadal dysgenesis, XY type - associated anomalies RGO:34244 RGO:34245 gonadal dysgenesis XY type RGO:34245 ORDO:1778 RGO:34247 facial dysmorphism - shawl scrotum - joint laxity RGO:34247 HP:0000049 RGO:34248 shawl scrotum RGO:34248 ORDO:1779 RGO:34249 dysmorphism - cleft palate - loose skin RGO:34249 DOID:3144 HP:0000973 RGO:34250 loose skin RGO:34250 ORDO:1780 RGO:34251 dysmorphism - multiple structural anomalies RGO:34251 RGO:34252 multiple structural anomalies RGO:34252 ORDO:1789 RGO:34253 craniofacial dysostosis - arthrogryposis - progeroid appearance RGO:34253 ORDO:1804 RGO:34254 dyssegmental dysplasia - glaucoma RGO:34254 ORDO:1806 RGO:34255 ectodermal dysplasia - blindness RGO:34255 ORDO:1812 RGO:34256 ectodermal dysplasia - intellectual deficit - central nervous system malformation RGO:34256 RGO:34257 central nervous system malformation RGO:34257 ORDO:1825 RGO:34258 epiphyseal dysplasia - hearing loss - dysmorphism RGO:34258 ORDO:1849 RGO:34259 infundibulopelvic stenosis - multicystic kidney RGO:34259 RGO:34260 infundibulopelvic stenosis RGO:34260 ORDO:1850 RGO:34261 renal dysplasia - megalocystis - sirenomelia RGO:34261 RGO:34262 megalocystis RGO:34262 ORDO:1856 RGO:34263 spondyloperipheral dysplasia - short ulna RGO:34263 ORDO:1858 RGO:34264 skeletal dysplasia - epilepsy - short stature RGO:34264 ORDO:1875 RGO:34265 congenital muscular dystrophy - infantile cataract - hypogonadism RGO:34265 SNOMEDCT:399120006 RGO:34266 infantile cataract RGO:34266 ORDO:1877 RGO:34267 muscular dystrophy - white matter spongiosis RGO:34267 RGO:34268 white matter spongiosis RGO:34268 ORDO:1882 RGO:34269 hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia RGO:34269 ORDO:1883 RGO:34270 ectodermal dysplasia - sensorineural deafness RGO:34270 ORDO:1884 RGO:34271 ectopia lentis - chorioretinal dystrophy - myopia RGO:34271 ORDO:1891 RGO:34272 intellectual deficit - spasticity - ectrodactyly RGO:34272 HP:0001257 SNOMEDCT:221360009 SNOMEDCT:397790002 RGO:34273 spasticity RGO:34273 ORDO:1892 RGO:34274 ectrodactyly - polydactyly RGO:34274 ORDO:1894 RGO:34275 ectrodactyly - spina bifida - cardiopathy RGO:34275 ORDO:1940 RGO:34276 shoulder and thorax deformity - congenital heart disease RGO:34276 RGO:34277 shoulder and thorax deformity RGO:34277 ORDO:1947 RGO:34278 progressive epilepsy - intellectual deficit Finnish type RGO:34278 RGO:34279 progressive epilepsy RGO:34279 ORDO:1948 RGO:34281 epilepsy - microcephaly - skeletal dysplasia RGO:34281 ORDO:1955 RGO:34282 erythrokeratodermia - ataxia RGO:34282 RGO:34283 erythrokeratodermia RGO:34283 ORDO:1962 RGO:34284 exostoses - anetodermia - brachydactyly type E RGO:34284 RGO:34285 anetodermia RGO:34285 ORDO:1964 RGO:34286 extrasystoles - short stature - hyperpigmentation - microcephaly RGO:34286 ICD10CM:I49.49 SNOMEDCT:29717002 RGO:34287 extrasystoles RGO:34287 ORDO:1968 RGO:34288 flat face - microstomia - ear anomaly RGO:34288 HP:0012368 RGO:34289 flat face RGO:34289 ORDO:1970 RGO:34290 facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation RGO:34290 ORDO:1995 RGO:34291 cleft lip - retinopathy RGO:34291 ORDO:2001 RGO:34292 cleft lip/palate - intestinal malrotation - cardiopathy RGO:34292 ORDO:2003 RGO:34293 cleft lip/palate - deafness - sacral lipoma RGO:34293 HP:0012033 RGO:34294 sacral lipoma RGO:34294 ORDO:2005 RGO:34295 laryngo-tracheo-esophageal cleft - pulmonary hypoplasia RGO:34295 ORDO:2004 RGO:34296 laryngo-tracheo-esophageal cleft RGO:34296 ORDO:2007 RGO:34297 alar cartilages hypoplasia - coloboma - telecanthus RGO:34297 RGO:34298 alar cartilages hypoplasia RGO:34298 ORDO:2010 RGO:34299 cleft palate - stapes fixation - oligodontia RGO:34299 RGO:34300 stapes fixation RGO:34300 ORDO:2013 RGO:34301 cleft palate - large ears - small head RGO:34301 HP:0000252 SNOMEDCT:271611007 RGO:34302 small head RGO:34302 ORDO:2015 RGO:34303 cleft palate - short stature - vertebral anomalies RGO:34303 ORDO:2027 RGO:34304 gingival fibromatosis - progressive deafness RGO:34304 RGO:34305 progressive deafness RGO:34305 ORDO:2031 RGO:34306 hepatic fibrosis - renal cysts - intellectual deficit RGO:34306 ORDO:2033 RGO:34308 multifocal muscular fibrosis - obstructed vessels RGO:34308 RGO:34309 multifocal muscular fibrosis RGO:34309 RGO:34310 obstructed vessels RGO:34310 ORDO:2042 RGO:34311 tracheo-esophageal fistula - hypospadias RGO:34311 ORDO:2055 RGO:34312 growth deficiency - brachydactyly - dysmorphism RGO:34312 ORDO:2057 RGO:34313 blepharophimosis - ptosis - esotropia - syndactyly - short stature RGO:34313 ORDO:2063 RGO:34314 splenogonadal fusion - limb defects - micrognathia RGO:34314 HP:0025410 SNOMEDCT:62042001 RGO:34315 splenogonadal fusion RGO:34315 ORDO:2064 RGO:34316 posterior fusion of lumbosacral vertebrae - blepharoptosis RGO:34316 HP:0005626 RGO:34317 posterior fusion of lumbosacral vertebrae RGO:34317 ORDO:2072 RGO:34318 Gaucher disease - ophthalmoplegia - cardiovascular calcification RGO:34318 HP:0011915 RGO:34319 cardiovascular calcification RGO:34319 ORDO:2076 RGO:34320 X-linked intellectual deficit - epilepsy RGO:34320 ORDO:2081 RGO:34321 cerebral gigantism - jaw cysts RGO:34321 RGO:34322 jaw cysts RGO:34322 ORDO:2083 RGO:34323 prominent glabella - microcephaly - hypogenitalism RGO:34323 HP:0002057 RGO:34324 prominent glabella RGO:34324 ORDO:2085 RGO:34325 glaucoma - sleep apnea RGO:34325 DOID:0050847 HP:0010535 ICD10CM:G47.3 SNOMEDCT:73430006 RGO:34326 sleep apnea RGO:34326 ORDO:2087 RGO:34327 glomerulonephritis - sparse hair - telangiectasis RGO:34327 DOID:1272 SNOMEDCT:112641009 RGO:34328 telangiectasis RGO:34328 ORDO:2091 RGO:34329 multinodular goiter - cystic kidney - polydactyly RGO:34329 DOID:0050489 HP:0005987 SNOMEDCT:237570007 RGO:34330 multinodular goiter RGO:34330 RGO:34331 cystic kidney RGO:34331 ORDO:2104 RGO:34332 dysmorphism - pectus carinatum - joint laxity RGO:34332 ORDO:2110 RGO:34333 hallux varus - preaxial polysyndactyly RGO:34333 HP:0008080 SNOMEDCT:274147008 RGO:34334 hallux varus RGO:34334 ORDO:2112 RGO:34335 follicular hamartoma - alopecia - cystic fibrosis RGO:34335 RGO:34336 follicular hamartoma RGO:34336 ORDO:2124 RGO:34337 cavernous hemangiomas of face - supraumbilical midline raphe RGO:34337 RGO:34338 cavernous hemangiomas of face RGO:34338 RGO:34339 supraumbilical midline raphe RGO:34339 ORDO:2129 RGO:34340 hemihypertrophy - intestinal web - corneal opacity RGO:34340 RGO:34341 intestinal web RGO:34341 ORDO:2141 RGO:34342 diaphragmatic defect - limb deficiency - skull defect RGO:34342 HP:0000775 RGO:34343 diaphragmatic defect RGO:34343 RGO:34344 limb deficiency RGO:34344 ORDO:2150 RGO:34345 Hirschsprung disease - type D brachydactyly RGO:34345 ORDO:2151 RGO:34346 Hirschsprung disease - ganglioneuroblastoma RGO:34346 ORDO:2153 RGO:34347 Hirschsprung disease - nail hypoplasia - dysmorphism RGO:34347 ORDO:2155 RGO:34348 Hirschsprung disease - deafness - polydactyly RGO:34348 ORDO:2156 RGO:34349 hirsutism - skeletal dysplasia - intellectual deficit RGO:34349 ORDO:2158 RGO:34350 histidinuria - renal tubular defect RGO:34350 HP:0000124 SNOMEDCT:7703001 RGO:34351 renal tubular defect RGO:34351 ORDO:2163 RGO:34352 holoprosencephaly - craniosynostosis RGO:34352 ORDO:2172 RGO:34353 microcephaly - glomerulonephritis - marfanoid habitus RGO:34353 ORDO:2180 RGO:34354 hydrocephalus - costovertebral dysplasia - Sprengel anomaly RGO:34354 RGO:34355 costovertebral dysplasia RGO:34355 HP:0000912 RGO:34356 Sprengel anomaly RGO:34356 ORDO:2181 RGO:34357 hydrocephaly - tall stature - joint laxity RGO:34357 ORDO:2183 RGO:34358 hydrocephalus - obesity - hypogonadism RGO:34358 ORDO:2184 RGO:34359 hydrocephaly - low-insertion umbilicus RGO:34359 RGO:34360 low-insertion umbilicus RGO:34360 ORDO:2186 RGO:34361 hydrocephalus - blue sclerae - nephropathy RGO:34361 ORDO:2196 RGO:34362 familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement RGO:34362 RGO:34363 severe ocular involvement RGO:34363 ORDO:2211 RGO:34364 hypertelorism - hypospadias - polysyndactyly syndrome RGO:34364 ORDO:2215 RGO:34365 malignant hyperthermia - arthrogryposis - torticollis RGO:34365 ORDO:2218 RGO:34366 cervical hypertrichosis - peripheral neuropathy RGO:34366 RGO:34367 cervical hypertrichosis RGO:34367 ORDO:2220 RGO:34368 hypertrichosis cubiti - short stature RGO:34368 ORDO:2228 RGO:34369 hypodontia - dysplasia of nails RGO:34369 ORDO:2229 RGO:34370 dilated cardiomyopathy - hypergonadotropic hypogonadism RGO:34370 DOID:12930 HP:0001644 ICD10CM:I42.0 RADLEX:RID3244 SNOMEDCT:399020009 RGO:34371 dilated cardiomyopathy RGO:34371 ORDO:2230 RGO:34372 hypogonadotropic hypogonadism - frontoparietal alopecia RGO:34372 RGO:34373 frontoparietal alopecia RGO:34373 ORDO:2232 RGO:34374 primary hypergonadotropic hypogonadism - partial alopecia RGO:34374 RGO:34375 primary hypergonadotropic hypogonadism RGO:34375 RGO:34376 partial alopecia RGO:34376 ORDO:2233 RGO:34377 hypogonadism - mitral valve prolapse - intellectual deficit RGO:34377 ORDO:2234 RGO:34378 male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies RGO:34378 RGO:34379 male hypergonadotropic hypogonadism RGO:34379 ORDO:2235 RGO:34380 hypogonadotropic hypogonadism - retinitis pigmentosa RGO:34380 ORDO:2237 RGO:34381 hypoparathyroidism - deafness - renal disease RGO:34381 ORDO:2246 RGO:34382 cerebellar hypoplasia - tapetoretinal degeneration RGO:34382 ORDO:2249 RGO:34383 ulna hypoplasia - intellectual deficit RGO:34383 RGO:34384 ulna hypoplasia RGO:34384 ORDO:2250 RGO:34385 hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism RGO:34385 RGO:34386 nasal and ocular hypoplasia RGO:34386 ORDO:2251 RGO:34387 thumb deformity - alopecia - pigmentation anomaly RGO:34387 HP:0001172 RGO:34388 thumb deformity RGO:34388 HP:0001000 RGO:34389 pigmentation anomaly RGO:34389 ORDO:2253 RGO:34390 foveal hypoplasia - presenile cataract RGO:34390 HP:0007750 RGO:34391 foveal hypoplasia RGO:34391 HP:0007819 SNOMEDCT:441622000 RGO:34392 presenile cataract RGO:34392 ORDO:2255 RGO:34393 pancreatic hypoplasia - diabetes - congenital heart disease RGO:34393 HP:0002594 SNOMEDCT:68591005 RGO:34394 pancreatic hypoplasia RGO:34394 ORDO:2261 RGO:34395 hypospadias - intellectual deficit Goldblatt type RGO:34395 ORDO:2269 RGO:34397 ichthyosis - alopecia - eclabion - ectropion - intellectual deficit RGO:34397 HP:0012472 RGO:34398 eclabion RGO:34398 ORDO:2271 RGO:34399 congenital ichthyosis - microcephalus - tetraplegia RGO:34399 DOID:1695 HP:0007431 ICD10CM:Q80 SNOMEDCT:13059002 RGO:34400 congenital ichthyosis RGO:34400 DOID:10907 SNOMEDCT:1829003 RGO:34401 microcephalus RGO:34401 DOID:12835 HP:0002445 SNOMEDCT:11538006 RGO:34402 tetraplegia RGO:34402 ORDO:2274 RGO:34403 ichthyosis - hepatosplenomegaly - cerebellar degeneration RGO:34403 HP:0001433 SNOMEDCT:36760000 RGO:34404 hepatosplenomegaly RGO:34404 SNOMEDCT:95646004 RGO:34405 cerebellar degeneration RGO:34405 ORDO:2278 RGO:34406 ichthyosis - intellectual deficit - dwarfism - renal impairment RGO:34406 SNOMEDCT:236423003 RGO:34407 renal impairment RGO:34407 ORDO:2282 RGO:34408 dysmorphism - short stature - deafness - disorder of sex development RGO:34408 RGO:34409 disorder of sex development RGO:34409 ORDO:2310 RGO:34410 absence deformity of leg - cataract RGO:34410 RGO:34411 absence deformity of leg RGO:34411 ORDO:2326 RGO:34412 Kallmann syndrome - heart disease RGO:34412 DOID:114 RADLEX:RID3234 SNOMEDCT:56265001 RGO:34413 heart disease RGO:34413 ORDO:2339 RGO:34414 keratosis follicularis - dwarfism - cerebral atrophy RGO:34414 DOID:2734 SNOMEDCT:48611009 RGO:34415 keratosis follicularis RGO:34415 ORDO:2349 RGO:34416 muscular pseudohypertrophy - hypothyroidism RGO:34416 RGO:34417 muscular pseudohypertrophy RGO:34417 ORDO:2370 RGO:34418 Larsen-like osseous dysplasia - short stature RGO:34418 RGO:34419 Larsen-like osseous dysplasia RGO:34419 ORDO:2375 RGO:34420 laryngeal abductor paralysis - intellectual deficit RGO:34420 RGO:34421 laryngeal abductor paralysis RGO:34421 ORDO:2379 RGO:34422 early-onset parkinsonism - intellectual deficit RGO:34422 RGO:34423 early-onset parkinsonism RGO:34423 ORDO:2400 RGO:34424 peripheral motor neuropathy - dysautonomia RGO:34424 DOID:683 HP:0007178 SNOMEDCT:95663000 RGO:34425 peripheral motor neuropathy RGO:34425 ORDO:2405 RGO:34426 thickened earlobes - conductive deafness RGO:34426 RGO:34427 thickened earlobes RGO:34427 ORDO:2410 RGO:34428 hypergonadotropic hypogonadism - cataract syndrome RGO:34428 ORDO:2412 RGO:34429 dislocation of the hip - dysmorphism RGO:34429 RGO:34430 dislocation of the hip RGO:34430 ORDO:2427 RGO:34431 macrocephaly - short stature - paraplegia RGO:34431 ORDO:2429 RGO:34432 macrocephaly - spastic paraplegia - dysmorphism RGO:34432 ORDO:2432 RGO:34433 macrosomia - microphthalmia - cleft palate RGO:34433 ORDO:2435 RGO:34434 hypomelanotic and hypermelanotic cutaneous macules - retarded growth - intellectual deficiency RGO:34434 RGO:34435 hypomelanotic and hypermelanotic cutaneous macules RGO:34435 HP:0001510 RGO:34436 retarded growth RGO:34436 ORDO:2437 RGO:34438 split hand - urinary anomalies - spina bifida RGO:34438 HP:0001171 RGO:34439 split hand RGO:34439 RGO:34440 urinary anomaly RGO:34440 ORDO:2454 RGO:34441 familial intestinal malrotation - facial anomalies RGO:34441 HP:0000271 RGO:34442 facial anomaly RGO:34442 ORDO:2458 RGO:34443 mandibulofacial dysostosis - deafness - postaxial polydactyly RGO:34443 ORDO:2463 RGO:34444 autosomal recessive marfanoid habitus - intellectual deficit RGO:34444 ORDO:2486 RGO:34446 transverse limb deficiency - hemangioma RGO:34446 RGO:34447 transverse limb deficiency RGO:34447 ORDO:2487 RGO:34448 lower limb deficiency - hypospadias RGO:34448 RGO:34449 lower limb deficiency RGO:34449 RGO:34450 radial defect RGO:34450 ORDO:2272 RGO:34451 ichthyosis - oral and digital anomalies RGO:34451 RGO:34452 oral anomaly RGO:34452 ORDO:2489 RGO:34453 upper limb defect - eye and ear abnormalities RGO:34453 RGO:34454 upper limb defect RGO:34454 RGO:34455 eye abnormality RGO:34455 RGO:34456 ear abnormality RGO:34456 ORDO:2491 RGO:34457 mullerian duct anomalies - limb anomalies RGO:34457 RGO:34458 mullerian duct anomaly RGO:34458 ORDO:2492 RGO:34459 limb transversal defect - cardiac anomaly RGO:34459 RGO:34460 limb transversal defect RGO:34460 RGO:34461 cardiac anomaly RGO:34461 ORDO:2508 RGO:34462 micrencephaly - corpus callosum agenesis - abnormal genitalia RGO:34462 RGO:34463 abnormal genitalia RGO:34463 ORDO:2511 RGO:34464 microbrachycephaly - ptosis - cleft lip RGO:34464 RGO:34465 microbrachycephaly RGO:34465 ORDO:2513 RGO:34466 microcephaly - albinism - digital anomalies RGO:34466 ORDO:2515 RGO:34467 microcephaly - cardiomyopathy RGO:34467 ORDO:2516 RGO:34468 microcephaly - cardiac defect - lung malsegmentation RGO:34468 RGO:34469 lung malsegmentation RGO:34469 ORDO:2519 RGO:34470 microcephaly - seizures - intellectual deficit - heart disease RGO:34470 ORDO:2521 RGO:34471 microcephaly - cleft palate RGO:34471 ORDO:2522 RGO:34472 microcephaly - cervical spine fusion anomalies RGO:34472 RGO:34473 cervical spine fusion anomaly RGO:34473 ORDO:2523 RGO:34474 microcephaly - brain defect - spasticity - hypernatremia RGO:34474 RGO:34475 brain defect RGO:34475 HP:0003228 SNOMEDCT:39355002 RGO:34476 hypernatremia RGO:34476 ORDO:2526 RGO:34477 microcephaly - lymphedema - chorioretinopathy RGO:34477 SNOMEDCT:302893000 RGO:34478 chorioretinopathy RGO:34478 ORDO:2533 RGO:34479 microcephaly - deafness - intellectual deficit RGO:34479 ORDO:2535 RGO:34480 microcornea - corectopia - macular hypoplasia RGO:34480 HP:0000482 ICD10CM:Q13.4 SNOMEDCT:26098002 RGO:34481 microcornea RGO:34481 HP:0009918 ICD10CM:Q13.2 SNOMEDCT:193523008 RGO:34482 corectopia RGO:34482 HP:0001104 RGO:34483 macular hypoplasia RGO:34483 ORDO:2536 RGO:34484 microcornea - glaucoma - absent frontal sinuses RGO:34484 HP:0002688 RGO:34485 absent frontal sinuses RGO:34485 ORDO:2542 RGO:34486 isolated anophthalmia - microphthalmia RGO:34486 RGO:34487 isolated anophthalmia RGO:34487 ORDO:2543 RGO:34488 microphthalmia - cataract RGO:34488 ORDO:2547 RGO:34489 microphthalmia - microtia - fetal akinesia RGO:34489 HP:0001989 RGO:34490 fetal akinesia RGO:34490 ORDO:2560 RGO:34491 Möbius syndrome - axonal neuropathy - hypogonadotropic hypogonadism RGO:34491 DOID:7319 HP:0003477 SNOMEDCT:60703000 RGO:34492 axonal neuropathy RGO:34492 ORDO:2572 RGO:34493 spastic ataxia - corneal dystrophy RGO:34493 DOID:0050952 HP:0002497 RGO:34494 spastic ataxia RGO:34494 ORDO:2575 RGO:34495 cystic fibrosis - gastritis - megaloblastic anemia RGO:34495 DOID:13382 HP:0001889 SNOMEDCT:53165003 RGO:34496 megaloblastic anemia RGO:34496 ORDO:2579 RGO:34497 muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus RGO:34497 ORDO:2580 RGO:34498 shoulder and girdle defects - familial intellectual deficit RGO:34498 RGO:34499 shoulder defect RGO:34499 RGO:34500 girdle defect RGO:34500 ORDO:2585 RGO:34501 ataxia - pancytopenia RGO:34501 ORDO:2589 RGO:34502 myoclonus - cerebellar ataxia - deafness RGO:34502 HP:0001336 ICD10CM:G25.3 SNOMEDCT:17450006 RGO:34503 myoclonus RGO:34503 ORDO:2590 RGO:34504 hereditary myoclonus - progressive distal muscular atrophy RGO:34504 RGO:34505 hereditary myoclonus RGO:34505 HP:0008955 RGO:34506 progressive distal muscular atrophy RGO:34506 ORDO:2597 RGO:34507 mitochondrial myopathy - lactic acidosis - deafness RGO:34507 ORDO:2601 RGO:34508 myopathy - growth delay - intellectual deficit - hypospadias RGO:34508 HP:0001510 SNOMEDCT:276617005 RGO:34509 growth delay RGO:34509 ORDO:2621 RGO:34510 low birth weight - dwarfism - dysgammaglobulinemia RGO:34510 HP:0001518 SNOMEDCT:276610007 RGO:34511 low birth weight RGO:34511 ORDO:2626 RGO:34512 hypopituitarism - short stature - skeletal anomalies RGO:34512 ORDO:2631 RGO:34513 mesomelic dwarfism - cleft palate - camptodactyly RGO:34513 ORDO:2649 RGO:34514 short stature - intellectual deficit - eye anomalies - cleft lip/palate RGO:34514 ORDO:2650 RGO:34515 dwarfism - intellectual deficit - eye abnormality RGO:34515 ORDO:2653 RGO:34516 osteochondrodysplatic nanism - deafness - retinitis pigmentosa RGO:34516 RGO:34517 osteochondrodysplatic nanism RGO:34517 ORDO:2666 RGO:34518 adult familial nephronophtisis - spastic quadriparesia RGO:34518 RGO:34519 nephronophtisis RGO:34519 RGO:34520 spastic quadriparesia RGO:34520 ORDO:2668 RGO:34521 nephropathy - deafness - hyperparathyroidism RGO:34521 ORDO:2669 RGO:34522 nephrosis - deafness - urinary tract - digital malformations RGO:34522 RGO:34524 digital malformation RGO:34524 ORDO:2675 RGO:34525 neuroaxonal dystrophy - renal tubular acidosis RGO:34525 DOID:2367 SNOMEDCT:230365004 RGO:34526 neuroaxonal dystrophy RGO:34526 ORDO:2680 RGO:34527 hypomyelination neuropathy - arthrogryposis RGO:34527 RGO:34528 hypomyelination neuropathy RGO:34528 ORDO:2690 RGO:34529 neutropenia - monocytopenia - deafness RGO:34529 DOID:1227 HP:0001875 ICD10CM:D70 SNOMEDCT:165517008 RGO:34530 neutropenia RGO:34530 HP:0012312 ICD10CM:D72.818 SNOMEDCT:165539005 RGO:34531 monocytopenia RGO:34531 ORDO:2694 RGO:34532 epidermal nevus - vitamin D resistant rickets RGO:34532 DOID:0050532 HP:0010816 SNOMEDCT:239107007 SNOMEDCT:25201003 RGO:34533 epidermal nevus RGO:34533 RGO:34534 vitamin D resistant rickets RGO:34534 ORDO:2703 RGO:34535 port-wine nevi - mega cisterna magna - hydrocephalus RGO:34535 RGO:34536 port-wine nevi RGO:34536 ORDO:2722 RGO:34537 odonto-onycho dysplasia - alopecia RGO:34537 RGO:34538 odonto-onycho dysplasia RGO:34538 Boder syndrome odontoma-dysphagia syndrome ORDO:2724 RGO:34539 odontomatosis - aortae esophagus stenosis RGO:34539 RGO:34540 odontomatosis RGO:34540 ORDO:2725 RGO:34543 eye defects - arachnodactyly - cardiopathy RGO:34543 RGO:34544 eye defect RGO:34544 ORDO:2731 RGO:34545 taurodontia - absent teeth - sparse hair RGO:34545 HP:0000679 RGO:34546 taurodontia RGO:34546 RGO:34547 absent teeth RGO:34547 ORDO:2732 RGO:34548 olivopontocerebellar atrophy - deafness RGO:34548 ORDO:2739 RGO:34549 onycho-tricho-dysplasia - neutropenia RGO:34549 RGO:34550 onycho-tricho-dysplasia RGO:34550 ORDO:2742 RGO:34551 ophthalmoplegia - myalgia - tubular aggregates RGO:34551 HP:0003326 ICD10CM:M79.1 SNOMEDCT:68962001 RGO:34552 myalgia RGO:34552 SNOMEDCT:43539003 RGO:34553 tubular aggregates RGO:34553 Levic-Stefanovic-Nikolic syndrome ORDO:2743 RGO:34554 ophthalmoplegia - intellectual deficit - lingua scrotalis RGO:34554 RGO:34555 lingua scrotalis RGO:34555 ORDO:2759 RGO:34557 imperforate oropharynx - costo vetebral anomalies RGO:34557 RGO:34558 imperforate oropharynx RGO:34558 RGO:34559 costovetebral anomaly RGO:34559 ORDO:2772 RGO:34560 congenital osteogenesis imperfecta - microcephaly - cataracts RGO:34560 RGO:34561 congenital osteogenesis imperfecta RGO:34561 ORDO:2773 RGO:34563 osteogenesis imperfecta - retinopathy - seizures - intellectual deficit RGO:34563 ORDO:2779 RGO:34564 osteopathia striata - pigmentary dermopathy - white forelock RGO:34564 RGO:34565 pigmentary dermopathy RGO:34565 ORDO:2786 RGO:34566 osteoporosis - oculocutaneous hypopigmentation syndrome RGO:34566 RGO:34567 oculocutaneous hypopigmentation RGO:34567 ORDO:2787 RGO:34568 osteoporosis - macrocephaly - blindness - joint hyperlaxity RGO:34568 ORDO:2795 RGO:34569 polycystic ovaries - urethral sphincter dysfunction RGO:34569 RGO:34570 urethral sphincter dysfunction RGO:34570 ORDO:2798 RGO:34571 pachygyria - intellectual deficit - epilepsy RGO:34571 ORDO:2802 RGO:34572 X-linked sideroblastic anemia - ataxia RGO:34572 DOID:8955 HP:0001924 SNOMEDCT:41841004 RGO:34573 sideroblastic anemia RGO:34573 ORDO:2815 RGO:34574 spastic paraparesis - deafness RGO:34574 HP:0002313 SNOMEDCT:312444006 RGO:34575 spastic paraparesis RGO:34575 ORDO:2816 RGO:34576 spastic paraplegia - epilepsy - intellectual deficit RGO:34576 ORDO:2818 RGO:34577 spastic paraplegia - glaucoma - intellectual deficit RGO:34577 ORDO:2819 RGO:34578 spastic paraplegia - facial-cutaneous lesions RGO:34578 RGO:34579 facial-cutaneous lesion RGO:34579 ORDO:2820 RGO:34580 spastic paraplegia - nephritis - deafness RGO:34580 ORDO:2821 RGO:34581 spastic paraplegia - neuropathy - poikiloderma RGO:34581 ORDO:2823 RGO:34582 paraplegia - brachydactyly - cone-shaped epiphysis RGO:34582 ORDO:2824 RGO:34583 paraplegia - intellectual deficit - hyperkeratosis RGO:34583 ORDO:2826 RGO:34584 spastic paraplegia - precocious puberty RGO:34584 ORDO:2832 RGO:34585 short tarsus - absence of lower eyelashes RGO:34585 RGO:34586 short tarsus RGO:34586 RGO:34587 absence of lower eyelashes RGO:34587 ORDO:2835 RGO:34588 pectus excavatum - macrocephaly - dysplastic nails RGO:34588 HP:0002164 RGO:34589 dysplastic nails RGO:34589 ORDO:2838 RGO:34590 renal caliceal diverticuli - deafness RGO:34590 RGO:34591 renal caliceal diverticuli RGO:34591 D'Ercole syndrome ORDO:2861 RGO:34592 short stature - microcephaly - heart defect RGO:34592 ORDO:2863 RGO:34594 short stature - wormian bones - dextrocardia RGO:34594 ORDO:2865 RGO:34595 short stature - webbed neck - heart disease RGO:34595 ORDO:2866 RGO:34596 short stature - deafness - neutrophil dysfunction - dysmorphism RGO:34596 ORDO:2868 RGO:34597 short stature - valvular heart disease - characteristic facies RGO:34597 ORDO:2878 RGO:34598 phocomelia - ectrodactyly - deafness - sinus arrhythmia RGO:34598 SNOMEDCT:71792006 RGO:34599 sinus arrhythmia RGO:34599 ORDO:2885 RGO:34600 piebald trait - neurologic defects RGO:34600 DOID:3263 RGO:34601 piebald trait RGO:34601 RGO:34602 neurologic defect RGO:34602 ORDO:2888 RGO:34603 Pierre Robin syndrome - faciodigital anomaly RGO:34603 RGO:34604 faciodigital anomaly RGO:34604 ORDO:2890 RGO:34605 pili torti - onychodysplasia RGO:34605 HP:0003777 SNOMEDCT:17170005 RGO:34606 pili torti RGO:34606 ORDO:2891 RGO:34607 pili torti - developmental delay - neurological abnormalities RGO:34607 HP:0000707 RGO:34608 neurological abnormality RGO:34608 ORDO:2892 RGO:34609 pilodental dysplasia - refractive errors RGO:34609 RGO:34610 pilodental dysplasia RGO:34610 DOID:9835 SNOMEDCT:39021009 RGO:34611 refractive error RGO:34611 ORDO:2898 RGO:34612 X-linked intellectual deficit - plagiocephaly RGO:34612 ORDO:2921 RGO:34613 preaxial polydactyly - colobomata - intellectual deficit RGO:34613 RGO:34614 colobomata RGO:34614 ORDO:2925 RGO:34615 polymicrogyria - turricephaly - hypogenitalism RGO:34615 ORDO:2926 RGO:34616 polyneuropathy - hand defect RGO:34616 RGO:34617 hand defect RGO:34617 ORDO:2928 RGO:34618 polyneuropathy - intellectual deficit - acromicria - premature menopause RGO:34618 RGO:34619 acromicria RGO:34619 DOID:10787 DOID:5426 HP:0008209 ICD10CM:E28.31 SNOMEDCT:373717006 RGO:34620 premature menopause RGO:34620 ORDO:2941 RGO:34621 porencephaly - cerebellar hypoplasia - internal malformations RGO:34621 RGO:34622 internal malformations RGO:34622 ORDO:2946 RGO:34623 brachydactyly - long thumb RGO:34623 RGO:34624 long thumb RGO:34624 ORDO:2947 RGO:34625 triphalangeal thumbs - brachyectrodactyly RGO:34625 RGO:34626 brachyectrodactyly RGO:34626 ORDO:2950 RGO:34627 triphalangeal thumb - polysyndactyly syndrome RGO:34627 ORDO:2951 RGO:34628 absent thumb - short stature - immunodeficiency RGO:34628 ORDO:2952 RGO:34629 adducted thumbs - arthrogryposis Christian type RGO:34629 HP:0001181 RGO:34630 adducted thumbs RGO:34630 RGO:34631 arthrogryposis Christian type RGO:34631 ORDO:2958 RGO:34632 X-linked intellectual deficit - dysmorphism - cerebral atrophy RGO:34632 ORDO:2959 RGO:34633 progeria - short stature - pigmented nevi RGO:34633 ORDO:2972 RGO:34634 non-eruption of teeth - maxillary hypoplasia - genu valgum RGO:34634 RGO:34635 non-eruption of teeth RGO:34635 ORDO:2973 RGO:34636 46,XX disorder of sex development - anorectal anomalies RGO:34636 RGO:34637 46,XX disorder of sex development RGO:34637 ORDO:2975 RGO:34638 46,XX disorder of sex development - skeletal anomalies RGO:34638 ORDO:2983 RGO:34639 disorder of sex development - intellectual deficit RGO:34639 ORDO:2988 RGO:34640 pterygium colli - intellectual deficit - digital anomalies RGO:34640 HP:0000465 ICD10CM:Q18.3 RGO:34641 pterygium colli RGO:34641 ORDO:2994 RGO:34642 short stature - craniofacial anomalies - genital hypoplasia RGO:34642 RGO:34643 craniofacial anomaly RGO:34643 Tucker syndrome ORDO:2997 RGO:34644 ptosis - vocal cord paralysis RGO:34644 ORDO:2999 RGO:34646 ptosis - strabismus - ectopic pupils RGO:34646 RGO:34647 ectopic pupils RGO:34647 ORDO:3004 RGO:34648 mirror polydactyly - vertebral segmentation - limbs defects RGO:34648 RGO:34649 mirror polydactyly RGO:34649 RGO:34650 vertebral segmentation disorder RGO:34650 RGO:34651 limb defect RGO:34651 ORDO:3011 RGO:34652 spastic tetraplegia - retinitis pigmentosa - intellectual deficit RGO:34652 HP:0002510 SNOMEDCT:192965001 RGO:34653 spastic tetraplegia RGO:34653 ORDO:3018 RGO:34654 retinal ischemic - digestive tract small vessel hyalinosis - diffuse cerebral calcifications RGO:34654 RGO:34655 digestive tract small vessel hyalinosis RGO:34655 HP:0005849 RGO:34656 diffuse cerebral calcification RGO:34656 ORDO:3026 RGO:34657 radial ray hypoplasia - choanal atresia RGO:34657 ORDO:3035 RGO:34658 growth delay - hydrocephaly - lung hypoplasia RGO:34658 HP:0002089 RGO:34659 lung hypoplasia RGO:34659 ORDO:3038 RGO:34660 delayed speech - facial asymmetry - strabismus - ear lobe creases RGO:34660 HP:0000750 RGO:34661 delayed speech RGO:34661 SNOMEDCT:418048009 RGO:34662 ear lobe crease RGO:34662 ORDO:3041 RGO:34663 intellectual deficit - balding - patella luxation - acromicria RGO:34663 SNOMEDCT:298000004 RGO:34664 balding RGO:34664 RGO:34665 patella luxation RGO:34665 ORDO:3042 RGO:34666 intellectual deficit - cataracts - calcified pinnae - myopathy RGO:34666 ORDO:3043 RGO:34668 intellectual deficit - unusual facies RGO:34668 ORDO:3044 RGO:34669 intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus RGO:34669 ORDO:3050 RGO:34670 intellectual deficit - hypotonia - skin hyperpigmentation RGO:34670 HP:0000953 RGO:34671 skin hyperpigmentation RGO:34671 ORDO:3051 RGO:34672 intellectual deficit - sparse hair - brachydactyly RGO:34672 ORDO:3052 RGO:34673 X-linked intellectual deficit - seizures - psoriasis RGO:34673 ORDO:3055 RGO:34674 X-linked intellectual deficit - short stature - obesity RGO:34674 ORDO:3067 RGO:34675 intellectual deficit - microcephaly - phalangeal - facial abnormalities RGO:34675 RGO:34676 phalangeal abnormality RGO:34676 ORDO:3068 RGO:34677 intellectual deficit - myopathy - short stature - endocrine defect RGO:34677 RGO:34678 endocrine defect RGO:34678 ORDO:3074 RGO:34679 intellectual deficit - short stature - hypertelorism RGO:34679 ORDO:3077 RGO:34680 X-linked intellectual deficit - psychosis - macroorchidism RGO:34680 HP:0000709 SNOMEDCT:69322001 RGO:34681 psychosis RGO:34681 ORDO:3082 RGO:34682 intellectual deficit - polydactyly - uncombable hair RGO:34682 ORDO:3085 RGO:34683 retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism RGO:34683 ORDO:3088 RGO:34684 retinopathy - anemia- central nervous system anomalies RGO:34684 RGO:34685 central nervous system anomaly RGO:34685 ORDO:3122 RGO:34686 sinus node disease - myopia RGO:34686 RGO:34687 sinus node disease RGO:34687 ORDO:3145 RGO:34688 nephrogenic diabetes insipidus - intracranial calcification RGO:34688 DOID:12387 HP:0009806 ICD10CM:N25.1 SNOMEDCT:111395007 RGO:34689 nephrogenic diabetes insipidus RGO:34689 ORDO:3151 RGO:34690 multiple sclerosis - ichthyosis - factor VIII deficiency RGO:34690 DOID:12134 HP:0003125 SNOMEDCT:234440005 RGO:34691 factor VIII deficiency RGO:34691 ORDO:3172 RGO:34692 eyebrow duplication - syndactyly RGO:34692 RGO:34693 eyebrow duplication RGO:34693 ORDO:3173 RGO:34694 infantile spasms - broad thumbs RGO:34694 HP:0012469 ICD10CM:G40.82 SNOMEDCT:28055006 RGO:34695 infantile spasms RGO:34695 ORDO:3175 RGO:34696 spasticity - intellectual deficit - X-linked epilepsy RGO:34696 ORDO:3176 RGO:34697 spina bifida - hypospadias RGO:34697 ORDO:3186 RGO:34698 holoprosencephaly - radial heart renal anomalies RGO:34698 RGO:34699 radial heart anomaly RGO:34699 ORDO:3196 RGO:34700 steroid dehydrogenase deficiency - dental anomalies RGO:34700 RGO:34701 steroid dehydrogenase deficiency RGO:34701 ORDO:3201 RGO:34702 ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence RGO:34702 RGO:34703 ventricular extrasystoles with syncopal episodes RGO:34703 RGO:34704 perodactyly RGO:34704 ORDO:3207 RGO:34705 white matter hypoplasia - corpus callosum agenesis - intellectual deficit RGO:34705 RGO:34706 white matter hypoplasia RGO:34706 ORDO:3215 RGO:34707 deafness - white hair - contractures - papillomas RGO:34707 HP:0011364 SNOMEDCT:297993006 RGO:34708 white hair RGO:34708 RGO:34709 papillomas RGO:34709 ORDO:3216 RGO:34710 conductive deafness - malformed external ear RGO:34710 RGO:34711 malformed external ear RGO:34711 ORDO:3217 RGO:34712 deafness - small bowel diverticulosis - neuropathy RGO:34712 ORDO:3218 RGO:34714 deafness - epiphyseal dysplasia - short stature RGO:34714 Tungland-Bellman syndrome ORDO:3225 RGO:34715 hearing loss - familial salivary gland insensitivity to aldosterone RGO:34715 RGO:34716 familial salivary gland insensitivity to aldosterone RGO:34716 ORDO:3226 RGO:34718 deafness - lymphedema - leukemia RGO:34718 ORDO:3228 RGO:34719 neurosensory deafness - pituitary dwarfism RGO:34719 SNOMEDCT:60700002 RGO:34720 neurosensory deafness RGO:34720 ORDO:3229 RGO:34721 deafness - peripheral neuropathy - arterial disease RGO:34721 SNOMEDCT:359557001 RGO:34722 arterial disease RGO:34722 ORDO:3230 RGO:34723 deafness - oligodontia RGO:34723 ORDO:3231 RGO:34724 deafness - onychodystrophy RGO:34724 ORDO:3232 RGO:34725 deafness - ear malformation - facial palsy RGO:34725 DOID:13934 HP:0010628 ICD10CM:G51.0 SNOMEDCT:280816001 RGO:34726 facial palsy RGO:34726 ORDO:3233 RGO:34727 cochleosaccular degeneration - cataract RGO:34727 RGO:34728 cochleosaccular degeneration RGO:34728 ORDO:3236 RGO:34729 conductive deafness - ptosis - skeletal anomalies RGO:34729 ORDO:3240 RGO:34730 central nervous system calcification - deafness - tubular acidosis - anemia RGO:34730 RGO:34731 central nervous system calcification RGO:34731 RGO:34732 tubular acidosis RGO:34732 ORDO:3263 RGO:34733 syngnathia - cleft palate RGO:34733 SNOMEDCT:403772000 RGO:34734 syngnathia RGO:34734 ORDO:3268 RGO:34735 synostosis - microcephaly - scoliosis RGO:34735 DOID:11971 RADLEX:RID6093 SNOMEDCT:1216008 RGO:34736 synostosis RGO:34736 ORDO:3270 RGO:34737 radio-ulnar synostosis - intellectual deficit - hypotonia RGO:34737 ORDO:3284 RGO:34738 tachycardia - hypertension - microphthalmos - hyperglycinuria RGO:34738 HP:0001649 SNOMEDCT:3424008 RGO:34739 tachycardia RGO:34739 ORDO:3293 RGO:34740 telecanthus - hypertelorism - strabismus - pes cavus RGO:34740 Bindewald-Ulmer-Müller syndrome ORDO:3304 RGO:34741 Fallot complex - intellectual deficit - growth delay RGO:34741 ORDO:3323 RGO:34743 thrombocytopenia - Robin sequence RGO:34743 Holmes-Collins syndrome ORDO:3328 RGO:34744 absent tibia - polydactyly - arachnoid cyst RGO:34744 Chitty-Hall-Webb syndrome ORDO:3331 RGO:34746 bowed tibiae - radial anomalies - osteopenia - fractures RGO:34746 RGO:34747 bowed tibiae RGO:34747 RGO:34748 radial anomaly RGO:34748 ORDO:3341 RGO:34750 torticollis - keloids - cryptorchidism - renal dysplasia RGO:34750 ORDO:3350 RGO:34751 tremor - nystagmus - duodenal ulcer RGO:34751 HP:0001337 SNOMEDCT:26079004 RGO:34752 tremor RGO:34752 Pinheiro-Freire Maia-Miranda syndrome ORDO:3353 RGO:34753 trichodermodysplasia - dental alterations RGO:34753 RGO:34754 trichodermodysplasia RGO:34754 ORDO:3357 RGO:34756 tricho-odonto-onychodysplasia - dominant syndactyly RGO:34756 RGO:34757 tricho-odonto-onychodysplasia RGO:34757 RGO:34758 dominant syndactyly RGO:34758 ORDO:3360 RGO:34759 trichodermal syndrome - intellectual deficit RGO:34759 RGO:34760 trichodermal RGO:34760 ORDO:3361 RGO:34761 trichodysplasia - xeroderma RGO:34761 HP:0002552 RGO:34762 trichodysplasia RGO:34762 ICD10CM:E50.8 SNOMEDCT:52475004 RGO:34763 xeroderma RGO:34763 ORDO:3362 RGO:34764 trichomegaly - cataract - hereditary spherocytosis RGO:34764 ORDO:3363 RGO:34765 trichomegaly - retina pigmentary degeneration - dwarfism RGO:34765 RGO:34766 retina pigmentary degeneration RGO:34766 ORDO:3365 RGO:34767 trigonocephaly - broad thumbs RGO:34767 HP:0011304 SNOMEDCT:249773003 RGO:34768 broad thumbs RGO:34768 ORDO:3368 RGO:34769 trigonocephaly - bifid nose - acral anomalies RGO:34769 RGO:34770 acral anomaly RGO:34770 ORDO:3369 RGO:34771 trigonocephaly - short stature - developmental delay RGO:34771 ORDO:3390 RGO:34772 proximal tubulopathy - diabetes mellitus - cerebellar ataxia RGO:34772 HP:0000114 RGO:34773 proximal tubulopathy RGO:34773 ORDO:3405 RGO:34774 umbilical cord ulceration - intestinal atresia RGO:34774 RGO:34775 umbilical cord ulceration RGO:34775 ORDO:3411 RGO:34776 double uterus - hemivagina - renal agenesis RGO:34776 HP:0003762 RGO:34777 double uterus RGO:34777 RGO:34778 hemivagina RGO:34778 ORDO:3433 RGO:34779 microcephaly - brachydactyly - kyphoscoliosis RGO:34779 ORDO:33001 RGO:34780 lymphedema - distichiasis RGO:34780 ORDO:37042 RGO:34781 X-linked immune dysregulation - polyendocrinopathy - enteropathy RGO:34781 HP:0002958 RGO:34782 immune dysregulation RGO:34782 RGO:34783 polyendocrinopathy RGO:34783 HP:0002242 RADLEX:RID5273 SNOMEDCT:85919009 RGO:34784 enteropathy RGO:34784 ORDO:46532 RGO:34785 hereditary persistence of fetal hemoglobin - beta-thalassemia RGO:34785 SNOMEDCT:191201002 RGO:34786 hereditary persistence of fetal hemoglobin RGO:34786 RGO:34787 beta-thalassemia RGO:34787 ORDO:46658 RGO:34788 primordial short stature - microdontia - opalescent and rootless teeth RGO:34788 RGO:34789 primordial short stature RGO:34789 HP:0011072 SNOMEDCT:109493006 RGO:34790 rootless teeth RGO:34790 ORDO:50810 RGO:34791 microlissencephaly - micromelia RGO:34791 RGO:34792 microlissencephaly RGO:34792 ORDO:50817 RGO:34793 Duane anomaly - myopathy - scoliosis RGO:34793 HP:0009921 RGO:34794 Duane anomaly RGO:34794 ORDO:52054 RGO:34795 craniosynostosis - intracranial calcifications RGO:34795 Graham-Cox syndrome ORDO:52055 RGO:34796 agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia RGO:34796 LAAHD Vuopala disease ORDO:53696 RGO:34798 lethal arthrogryposis - anterior horn cell disease RGO:34798 RGO:34799 lethal arthrogryposis RGO:34799 DOID:4873 HP:0006802 SNOMEDCT:85672005 RGO:34800 anterior horn cell disease RGO:34800 IHSC NISCH syndrome ORDO:59303 RGO:34803 ichthyosis - hypotrichosis - sclerosing cholangitis RGO:34803 pancreatic and cerebellar agenesis ORDO:65288 RGO:34806 permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis RGO:34806 DOID:0060639 SNOMEDCT:609565001 RGO:34807 permanent neonatal diabetes mellitus RGO:34807 DOID:0050877 RGO:34808 pancreatic agenesis RGO:34808 distal arthrogryposis type 4 ORDO:65720 RGO:34810 arthrogryposis - severe scoliosis RGO:34810 DOID:0060249 HP:0002650 ICD10CM:M41 RADLEX:RID4756 SNOMEDCT:298382003 RGO:34811 scoliosis RGO:34811 ORDO:66633 RGO:34813 sensorineural hearing loss - early greying - essential tremor RGO:34813 RGO:34814 early greying RGO:34814 DOID:4990 HP:0030186 ICD10CM:G25.0 SNOMEDCT:609558009 RGO:34815 essential tremor RGO:34815 OL-EDA-ID syndrome ORDO:69088 RGO:34816 anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema RGO:34816 PAPA syndrome familial recurrent arthritis ORDO:69126 RGO:34818 pyogenic arthritis - pyoderma gangrenosum - acne RGO:34818 SANDO ORDO:70595 RGO:34821 sensory ataxic neuropathy - dysarthria - ophthalmoparesis RGO:34821 HP:0003434 RGO:34822 sensory ataxic neuropathy RGO:34822 HP:0000597 RGO:34823 ophthalmoparesis RGO:34823 ORDO:71267 RGO:34825 dentinogenesis imperfecta - short stature - hearing loss - intellectual deficit RGO:34825 ORDO:71270 RGO:34826 auriculoocular anomalies - cleft lip RGO:34826 ORDO:71271 RGO:34827 split hand - split foot - deafness RGO:34827 ORDO:73220 RGO:34828 X-linked intellectual deficit - hypotonic face RGO:34828 RGO:34829 hypotonic face RGO:34829 ORDO:73223 RGO:34830 global developmental delay - osteopenia - ectodermal defect RGO:34830 HP:0001263 ICD10CM:F88 SNOMEDCT:224958001 RGO:34831 global developmental delay RGO:34831 ORDO:73224 RGO:34832 tubular renal disease - cardiomyopathy RGO:34832 RGO:34833 tubular renal disease RGO:34833 HANAC syndrome hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome ORDO:73229 RGO:34834 autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures RGO:34834 HP:0001136 RGO:34835 retinal arteriolar tortuosity RGO:34835 ORDO:73230 RGO:34838 ossification anomalies - psychomotor development delay RGO:34838 RGO:34839 ossification anomaly RGO:34839 RGO:34840 psychomotor development delay RGO:34840 ORDO:73245 RGO:34841 spinal muscular atrophy - Dandy-Walker complex - cataracts RGO:34841 RGO:34842 Dandy-Walker complex RGO:34842 ORDO:73246 RGO:34843 visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay RGO:34843 RGO:34844 visceral neuropathy RGO:34844 sclerosing dysplasia of bone - ichthyosis - premature ovarian failure ORDO:75325 RGO:34845 osteosclerosis - ichthyosis - premature ovarian failure RGO:34845 DOID:5426 HP:0008209 SNOMEDCT:237788002 RGO:34846 premature ovarian failure RGO:34846 Goossens-Devriendt syndrome ORDO:75389 RGO:34848 brain malformation - congenital heart disease - postaxial polydactyly RGO:34848 RGO:34849 brain malformation RGO:34849 MCOPS3 syndromic microphthalmia type 3 ORDO:77298 RGO:34851 anophthalmia/microphthalmia - esophageal atresia RGO:34851 MCOPS10 MOBA syndrome syndromic microphthalmia type 10 ORDO:77299 RGO:34854 microphthalmia - brain atrophy RGO:34854 ORDO:77300 RGO:34858 auricular abnormalities - cleft lip with or without cleft palate - ocular abnormalities RGO:34858 IBM3 inclusion body myopathy type 3 ORDO:79091 RGO:34859 hereditary inclusion body myopathy - joint contractures - ophthalmoplegia RGO:34859 ORDO:79107 RGO:34862 developmental malformations - deafness - dystonia RGO:34862 SNOMEDCT:21390004 RGO:34863 developmental malformation RGO:34863 ORDO:79118 RGO:34864 neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys RGO:34864 RGO:34865 neonatal diabetes RGO:34865 VODI syndrome ORDO:79124 RGO:34866 hepatic veno-occlusive disease - immunodeficiency RGO:34866 RB-ILD ORDO:79127 RGO:34868 respiratory bronchiolitis - interstitial lung disease RGO:34868 DOID:3082 HP:0006530 RADLEX:RID28799 SNOMEDCT:233703007 RGO:34869 interstitial lung disease RGO:34869 ORDO:79129 RGO:34871 trichodysplasia - amelogenesis imperfecta RGO:34871 ORDO:79132 RGO:34872 sparse hair - short stature - skin anomalies RGO:34872 GEPD ORDO:79137 RGO:34873 generalized epilepsy - paroxysmal dyskinesia RGO:34873 SNOMEDCT:19598007 RGO:34874 generalized epilepsy RGO:34874 HP:0007166 RGO:34875 paroxysmal dyskinesia RGO:34875 ORDO:79156 RGO:34877 seizures - intellectual deficit due to hydroxylysinuria RGO:34877 RGO:34878 hydroxylysinuria RGO:34878 DDOD syndrome ORDO:79499 RGO:34879 autosomal dominant deafness - onychodystrophy syndrome RGO:34879 LTC4 synthase deficiency leukotriene C4 synthase deficiency ORDO:79507 RGO:34881 hypotonia - failure to thrive - microcephaly RGO:34881 ORDO:83617 RGO:34884 agammaglobulinemia - microcephaly - craniosynostosis - severe dermatitis RGO:34884 RGO:34885 severe dermatitis RGO:34885 ORDO:83619 RGO:34886 macrostomia - preauricular tags - external ophthalmoplegia RGO:34886 HP:0000384 RGO:34887 preauricular tags RGO:34887 ORDO:83629 RGO:34888 leukoencephalopathy - metaphyseal chondrodysplasia RGO:34888 ORDO:83648 RGO:34889 X-linked recessive intellectual deficit - macrocephaly - ciliary dysfunction RGO:34889 RGO:34890 ciliary dysfunction RGO:34890 palmoplantar hyperkeratosis - XX sex reversal - predisposition to squamous cell carcinoma ORDO:85112 RGO:34891 palmoplantar keratoderma - XX sex reversal - predisposition to squamous cell carcinoma RGO:34891 RGO:34892 predisposition to squamous cell carcinoma RGO:34892 ORDO:85163 RGO:34894 hypomyelination - congenital cataract RGO:34894 HP:0003429 SNOMEDCT:111007000 RGO:34895 hypomyelination RGO:34895 CATSHL syndrome ORDO:85164 RGO:34896 camptodactyly - tall stature - scoliosis - hearing loss RGO:34896 RGO:34898 severe achondroplasia RGO:34898 MCOPS4 syndromic microphthalmia type 4 ORDO:85275 RGO:34899 microphthalmia - ankyloblepharon - intellectual deficit RGO:34899 ORDO:85280 RGO:34902 X-linked intellectual deficit - cubitus valgus - dysmorphism RGO:34902 ORDO:85294 RGO:34903 X-linked epilepsy - learning disabilities - behavior disorders RGO:34903 DOID:8927 SNOMEDCT:1855002 SNOMEDCT:408468001 RGO:34904 learning disability RGO:34904 RGO:34905 behavior disorder RGO:34905 syndromic X-linked intellectual disability type 10 ORDO:85295 RGO:34906 X-linked intellectual deficit - choreoathetosis - abnormal behavior RGO:34906 HP:0001266 SNOMEDCT:43105007 RGO:34907 choreoathetosis RGO:34907 SNOMEDCT:25786006 RGO:34908 abnormal behavior RGO:34908 ORDO:85317 RGO:34910 X-linked intellectual deficit - hypogammaglobulinemia - progressive neurological deterioration RGO:34910 ORDO:85318 RGO:34912 X-linked intellectual deficit - precocious puberty - obesity RGO:34912 ORDO:85319 RGO:34913 X-linked intellectual deficit - epilepsy - progressive joint contractures - dysmorphism RGO:34913 Johnson syndrome ORDO:85320 RGO:34914 X-linked intellectual deficit - macrocephaly - macro-orchidism RGO:34914 Martin-Probst syndrome X-linked deafness - intellectual deficit syndrome ORDO:85321 RGO:34916 deafness - intellectual deficit Martin-Probst type RGO:34916 ORDO:85327 RGO:34919 X-linked intellectual deficit - acromegaly - hyperactivity RGO:34919 HP:0000752 RGO:34920 hyperactivity RGO:34920 ORDO:85329 RGO:34921 X-linked intellectual deficit - hypotonia - facial dysmorphism - aggressive behavior RGO:34921 HP:0000718 SNOMEDCT:61372001 RGO:34922 aggressive behavior RGO:34922 ORDO:85330 RGO:34923 X-linked intellectual deficit - corpus callosum agenesis - spastic quadriparesis RGO:34923 ORDO:85331 RGO:34924 X-linked intellectual deficit - hypogonadism - ichthyosis - obesity - short stature RGO:34924 ORDO:85338 RGO:34925 X-linked intellectual deficit - ataxia - apraxia RGO:34925 DOID:0060135 HP:0002186 ICD10CM:R48.2 SNOMEDCT:68345001 RGO:34926 apraxia RGO:34926 ORDO:85442 RGO:34927 short stature - pituitary and cerebellar defects - small sella turcica RGO:34927 RGO:34928 pituitary defect RGO:34928 RGO:34929 cerebellar defect RGO:34929 AMME syndrome ORDO:86818 RGO:34930 Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis RGO:34930 HP:0011800 RGO:34931 midface hypoplasia RGO:34931 ORDO:86821 RGO:34934 lissencephaly type 3 - familial fetal akinesia sequence RGO:34934 RGO:34935 lissencephaly type 3 RGO:34935 RGO:34936 familial fetal akinesia sequence RGO:34936 ORDO:86822 RGO:34937 lissencephaly type 3 - metacarpal bone dysplasia RGO:34937 RGO:34938 metacarpal bone dysplasia RGO:34938 ORDO:86914 RGO:34939 lymphedema - cerebral arteriovenous anomaly RGO:34939 RGO:34940 cerebral arteriovenous anomaly RGO:34940 Irons-Bianchi syndrome ORDO:86915 RGO:34941 lymphedema - atrial septal defects - facial changes RGO:34941 RGO:34942 facial changes RGO:34942 palmoplantar keratoderma - clinodactyly ORDO:86919 RGO:34944 keratosis palmaris et plantaris - clinodactyly RGO:34944 DOID:3390 RGO:34945 keratosis palmaris et plantaris RGO:34945 PCARP autosomal recessive posterior column ataxia and retinitis pigmentosa ORDO:88628 RGO:34947 posterior column ataxia - retinitis pigmentosa RGO:34947 RGO:34948 posterior column ataxia RGO:34948 ORDO:88636 RGO:34951 aortic dilatation - joint hypermobility - arterial tortuosity RGO:34951 4H syndrome ORDO:88637 RGO:34952 hypomyelination - hypogonadotropic hypogonadism - hypodontia RGO:34952 ORDO:88643 RGO:34954 obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay RGO:34954 ICD10CM:I51.7 RGO:34955 cardiac hypertrophy RGO:34955 ORDO:90022 RGO:34956 cardiomyopathy - renal anomalies RGO:34956 hereditary motor and sensory neuropathy with deafness, intellectual deficit and absent sensory large myelinated fibers ORDO:90103 RGO:34957 Charcot-Marie-Tooth disease - deafness - intellectual deficit RGO:34957 ORDO:90301 RGO:34959 acanthosis nigricans - Insulin resistance - muscle cramps - acral enlargement RGO:34959 HP:0000855 SNOMEDCT:48606007 RGO:34960 Insulin resistance RGO:34960 HP:0003394 SNOMEDCT:55300003 RGO:34961 muscle cramps RGO:34961 RGO:34962 acral enlargement RGO:34962 ORDO:90390 RGO:34963 anonychia - onychodystrophy RGO:34963 ORDO:91130 RGO:34964 cardiomyopathy - hypotonia - lactic acidosis RGO:34964 ORDO:91133 RGO:34965 osteopenia - myopia - hearing loss - intellectual deficit - facial dysmorphism RGO:34965 ORDO:91494 RGO:34966 macular coloboma - cleft palate - hallux valgus RGO:34966 Crouzono-dermoskeletal syndrome ORDO:93262 RGO:34967 Crouzon syndrome - acanthosis nigricans RGO:34967 ORDO:93951 RGO:34969 X-linked dominant intellectual deficit - epilepsy RGO:34969 MRXSH ORDO:93952 RGO:34970 X-linked recessive intellectual deficit - epilepsy RGO:34970 Meige dystonia Meige syndrome ORDO:93964 SNOMEDCT:230325003 RGO:34972 blepharospasm - oromandibular dystonia RGO:34972 DOID:529 HP:0000643 ICD10CM:G24.5 SNOMEDCT:59026006 RGO:34973 blepharospasm RGO:34973 DOID:0050843 HP:0012048 RGO:34974 oromandibular dystonia RGO:34974 ORDO:94061 RGO:34977 macrocephaly - immune deficiency - anemia RGO:34977 HP:0002721 RGO:34978 immune deficiency RGO:34978 ORDO:94062 RGO:34979 coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis RGO:34979 ORDO:94066 RGO:34980 severe intellectual deficit - epilepsy - anal anomalies - distal phalangeal hypoplasia RGO:34980 RGO:34981 severe intellectual deficit RGO:34981 RGO:34982 anal anomaly RGO:34982 HP:0009882 RGO:34983 distal phalangeal hypoplasia RGO:34983 Fryns-Aftimos syndrome cerebro-oculo-facial-lymphatic syndrome ORDO:94084 RGO:34984 pachygyria - epilepsy - intellectual deficit - dysmorphism RGO:34984 RGO:34988 anal malformation RGO:34988 RGO:34989 genitourinary malformation RGO:34989 SCAR3 ORDO:95433 RGO:34990 autosomal recessive cerebellar ataxia - blindness - deafness RGO:34990 SCAR4 SCASI ORDO:95434 RGO:34992 autosomal recessive cerebellar ataxia - saccadic intrusion RGO:34992 RGO:34993 saccadic intrusion RGO:34993 ATR-16 syndrome alpha thalassemia - retardation syndrome ORDO:98791 RGO:34996 alpha thalassemia - intellectual deficit syndrome linked to chromosome 16 RGO:34996 APV/PDA non-Fallot type PVA/PDA non-Fallot type ORDO:99048 RGO:34999 pulmonary valve agenesis - ventricular septal defect - persistent ductus arteriosus RGO:34999 RGO:35000 pulmonary valve agenesis RGO:35000 HP:0001643 ICD10CM:Q25.0 SNOMEDCT:253686000 RGO:35001 persistent ductus arteriosus RGO:35001 CAVC type A complete atrioventricular canal type A ORDO:99066 RGO:35004 complete atrioventricular canal - left heart obstruction RGO:35004 RGO:35005 left heart obstruction RGO:35005 CAVC type B complete atrioventricular canal type B ORDO:99067 RGO:35008 complete atrioventricular canal - ventricle hypoplasia RGO:35008 RGO:35009 ventricle hypoplasia RGO:35009 CAVC type C complete atrioventricular canal type C ORDO:99068 RGO:35012 complete atrioventricular canal - Fallot tetralogy RGO:35012 ORDO:99141 RGO:35015 posterior choanal atresia - lymphedema syndrome RGO:35015 DOID:9574 HP:0004496 RGO:35016 posterior choanal atresia RGO:35016 ORDO:99142 RGO:35017 microcephaly - cutis verticis gyrata - lymphedema RGO:35017 ORDO:99143 RGO:35018 mandibulofacial dysostosis - lymphedema syndrome RGO:35018 ORDO:101033 RGO:35019 Peters anomaly - cataract RGO:35019 APV/ADA Fallot type PVA/ADA Fallot type ORDO:101206 RGO:35020 pulmonary valve agenesis - Fallot tetralogy - absence of ductus arteriosus RGO:35020 RGO:35021 Fallot tetralogy RGO:35021 RGO:35022 absence of ductus arteriosus RGO:35022 ORDO:101356 RGO:35025 lissencephaly - demyelinating axonal neuropathy RGO:35025 RGO:35026 demyelinating axonal neuropathy RGO:35026 ORDO:103912 RGO:35027 epithelio-exfoliative colitis - deafness RGO:35027 RGO:35028 epithelio-exfoliative colitis RGO:35028 SOLAMEN syndrome ORDO:137608 RGO:35029 segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus RGO:35029 RGO:35030 segmental outgrowth RGO:35030 ORDO:137622 RGO:35032 intractable diarrhea - choanal atresia - eye anomalies RGO:35032 HP:0002041 RGO:35033 intractable diarrhea RGO:35033 ORDO:137628 RGO:35034 cardiac anomalies - heterotaxy RGO:35034 ORDO:137631 RGO:35035 lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis RGO:35035 RGO:35036 lung fibrosis RGO:35036 RGO:35037 46,XX gonadal dysgenesis RGO:35037 RNF135-related overgrowth syndrome ORDO:137634 RGO:35038 overgrowth - macrocephaly - facial dysmorphism RGO:35038 HP:0001548 RGO:35039 overgrowth RGO:35039 ataxia - delayed dentition - hypomyelination ORDO:137639 RGO:35041 leukoencephalopathy - ataxia - hypodontia - hypomyelination RGO:35041 Kelly-Kirson-Wyatt syndrome ORDO:137653 RGO:35043 microcephaly - digital anomalies - intellectual deficit RGO:35043 Woods-Crouchman-Huson syndrome ORDO:137658 RGO:35045 microcephaly - intellectual deficit - phalangeal and neurological anomalies RGO:35045 RGO:35046 phalangeal anomaly RGO:35046 RGO:35047 neurological anomaly RGO:35047 CM-AVM ORDO:137667 RGO:35049 capillary malformation - arteriovenous malformation RGO:35049 HP:0025104 RADLEX:RID3346 SNOMEDCT:234118009 RGO:35050 capillary malformation RGO:35050 OPHN1 syndrome oligophrenin-1 syndrome ORDO:137831 RGO:35052 X-linked intellectual deficit - cerebellar hypoplasia RGO:35052 LBSL ORDO:137898 RGO:35055 leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation RGO:35055 RGO:35056 lactate elevation RGO:35056 ORDO:137911 RGO:35058 autism - facial port-wine stain RGO:35058 RGO:35059 facial port-wine stain RGO:35059 Balikova-Vermeesch syndrome ORDO:139450 RGO:35060 microtia - eye coloboma - imperforation of the nasolacrimal duct RGO:35060 RGO:35061 imperforation of the nasolacrimal duct RGO:35061 STAR syndrome ORDO:140952 RGO:35063 syndactyly - telecanthus - anogenital and renal malformations RGO:35063 RGO:35064 anogenital malformation RGO:35064 HP:0012210 RGO:35065 renal malformation RGO:35065 ORDO:140963 RGO:35067 bilateral microtia - deafness - cleft palate RGO:35067 HP:0008551 RGO:35068 bilateral microtia RGO:35068 ORDO:157788 RGO:35069 hypospadias - hypertelorism - coloboma and deafness RGO:35069 ORDO:163681 RGO:35070 cortical dysplasia - focal epilepsy syndrome RGO:35070 HP:0002539 SNOMEDCT:253153000 RGO:35071 cortical dysplasia RGO:35071 DOID:2234 SNOMEDCT:230381009 RGO:35072 focal epilepsy RGO:35072 ORDO:163684 RGO:35073 leukoencephalopathy - dystonia - motor neuropathy RGO:35073 ORDO:163690 RGO:35074 hypotonia - cystinuria syndrome RGO:35074 ORDO:163696 RGO:35076 action myoclonus - renal failure syndrome RGO:35076 SNOMEDCT:27572006 RGO:35077 action myoclonus RGO:35077 ORDO:163721 RGO:35078 rolandic epilepsy - speech dyspraxia RGO:35078 DOID:3329 RGO:35079 rolandic epilepsy RGO:35079 RGO:35080 speech dyspraxia RGO:35080 ORDO:163727 RGO:35081 rolandic epilepsy - paroxysmal exercise-induced dystonia - writer's cramp RGO:35081 RGO:35082 paroxysmal exercise-induced dystonia RGO:35082 HP:0002356 SNOMEDCT:52008007 RGO:35083 writer's cramp RGO:35083 ORDO:163979 RGO:35084 X-linked intellectual deficit - craniofacioskeletal RGO:35084 RGO:35085 craniofacioskeletal syndrome RGO:35085 ORDO:163982 RGO:35086 X-linked intellectual deficit - spastic quadriparesis RGO:35086 ORDO:163985 RGO:35087 hyperekplexia - epilepsy RGO:35087 DOID:0060695 HP:0002267 SNOMEDCT:19557000 RGO:35088 hyperekplexia RGO:35088 ORDO:163988 RGO:35089 developmental delay - deafness Hildebrand type RGO:35089 RGO:35090 deafness Hildebrand type RGO:35090 ORDO:166035 RGO:35091 metaphyseal chondrodysplasia - retinitis pigmentosa RGO:35091 ORDO:168443 RGO:35092 spondyloepimetaphyseal dysplasia - hypotrichosis RGO:35092 ORDO:168451 RGO:35093 spondyloepimetaphyseal dysplasia - abnormal dentition RGO:35093 HP:0000164 RGO:35094 abnormal dentition RGO:35094 XY sex reversal - adrenal failure ORDO:168558 RGO:35095 46,XY disorder of sex development - adrenal insufficiency due to CYP11A1 deficiency RGO:35095 RGO:35096 46,XY disorder of sex development RGO:35096 RGO:35097 CYP11A1 deficiency RGO:35097 ORDO:168563 RGO:35099 46,XY gonadal dysgenesis - motor and sensory neuropathy RGO:35099 HP:0008668 RGO:35100 46,XY gonadal dysgenesis RGO:35100 SIDDT ORDO:168593 RGO:35101 sudden infant death - dysgenesis of the testes RGO:35101 SNOMEDCT:160957000 RGO:35102 sudden infant death RGO:35102 RGO:35103 dysgenesis of the testes RGO:35103 winged helix deficiency ORDO:169095 RGO:35105 severe T-cell immunodeficiency - congenital alopecia - nail dystrophy RGO:35105 HP:0005352 RGO:35106 severe T-cell immunodeficiency RGO:35106 ICD10CM:Q84.0 SNOMEDCT:2965006 RGO:35107 congenital alopecia RGO:35107 autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia autosomal recessive osteopetrosis type 7 ORDO:178389 RGO:35109 osteopetrosis - hypogammaglobulinemia RGO:35109 ORDO:199337 RGO:35112 pancreatic insufficiency - anemia - hyperostosis RGO:35112 ORDO:210133 RGO:35113 leukonychia totalis - acanthosis-nigricans-like lesions - abnormal hair RGO:35113 RGO:35114 acanthosis-nigricans-like lesions RGO:35114 RGO:35115 abnormal hair RGO:35115 ORDO:210136 RGO:35116 pulmonary fibrosis - hepatic hyperplasia - bone marrow hypoplasia RGO:35116 RGO:35117 hepatic hyperplasia RGO:35117 HP:0005528 SNOMEDCT:416995001 RGO:35118 bone marrow hypoplasia RGO:35118 Hadziselimovic syndrome ORDO:217026 RGO:35119 microcephaly - facio-cardio-skeletal syndrome Hadziselimovic type RGO:35119 RGO:35120 facio-cardio-skeletal syndrome Hadziselimovic type RGO:35120 FJHN type 2 familial juvenile hyperuricemic nephropathy type 2 ORDO:217330 RGO:35122 hyperuricemia - anemia - renal failure RGO:35122 progressive neurosensory deafness - hypertrophic cardiomyopathy progressive sensorineural deafness - hypertrophic cardiomyopathy ORDO:228012 RGO:35125 progressive sensorineural hearing loss - hypertrophic cardiomyopathy RGO:35125 RGO:35126 progressive sensorineural deafness RGO:35126 patent arterial duct - bicuspid aortic valve - hand anomalies ORDO:228190 RGO:35129 patent ductus arteriosus - bicuspid aortic valve - hand anomalies RGO:35129 ORDO:228396 RGO:35131 ptosis - upper ocular movement limitation - absence of lacrimal punctum RGO:35131 RGO:35132 upper ocular movement limitation RGO:35132 RGO:35133 absence of lacrimal punctum RGO:35133 MCSZ ORDO:228418 RGO:35134 microcephaly - seizures - developmental delay RGO:35134 C - beta-thalassemia HbC - beta-thalassemia ORDO:231242 RGO:35136 hemoglobin C - beta-thalassemia RGO:35136 SNOMEDCT:61967003 RGO:35137 hemoglobin C RGO:35137 E - beta-thalassemia HbE - beta-thalassemia ORDO:231249 RGO:35140 hemoglobin E - beta-thalassemia RGO:35140 SNOMEDCT:83815000 RGO:35141 hemoglobin E RGO:35141 ORDO:231256 RGO:35144 beta-thalassemia - trichothiodystrophy RGO:35144 XLTT ORDO:231393 RGO:35145 beta-thalassemia - X-linked thrombocytopenia RGO:35145 ATMDS acquired hemoglobin H disease ORDO:231401 RGO:35147 alpha-thalassemia - myelodysplastic syndrome RGO:35147 RGO:35148 myelodysplastic RGO:35148 ORDO:231556 RGO:35151 late-onset localized junctional epidermolysis bullosa - intellectual deficit RGO:35151 RGO:35152 late-onset localized junctional epidermolysis bullosa RGO:35152 MPPC syndrome ORDO:231736 RGO:35153 microcornea - posterior megalolenticonus - persistent fetal vasculature - coloboma RGO:35153 RGO:35154 posterior megalolenticonus RGO:35154 HP:0007968 RGO:35155 persistent fetal vasculature RGO:35155 ORDO:231742 RGO:35157 epibulbar lipodermoid - preauricular appendage - polythelia RGO:35157 RGO:35158 epibulbar lipodermoid RGO:35158 SNOMEDCT:204245004 RGO:35159 preauricular appendage RGO:35159 SNOMEDCT:50956007 RGO:35160 polythelia RGO:35160 atypical HCS ORDO:238523 RGO:35161 atypical hypotonia - cystinuria syndrome RGO:35161 RGO:35162 atypical hypotonia RGO:35162 ORDO:238766 RGO:35164 ptosis - syndactyly - learning difficulties RGO:35164 SNOMEDCT:161129001 RGO:35165 learning difficulties RGO:35165 PSP-p PSP-parkinsonism ORDO:240085 RGO:35166 progressive supranuclear palsy - parkinsonism RGO:35166 PSP-PAGF PSP-pure akinesia with gait freezing ORDO:240094 RGO:35169 progressive supranuclear palsy - pure akinesia with gait freezing RGO:35169 RGO:35170 pure akinesia with gait freezing RGO:35170 PSP-CBS PSP-corticobasal syndrome ORDO:240103 RGO:35173 progressive supranuclear palsy - corticobasal syndrome RGO:35173 RGO:35174 corticobasal syndrome RGO:35174 PSP-PNFA progressive supranuclear palsy - apraxia of speech ORDO:240112 RGO:35177 progressive supranuclear palsy - progressive nonfluent aphasia RGO:35177 RGO:35178 progressive nonfluent aphasia RGO:35178 ORDO:247522 RGO:35181 primary ciliary dyskinesia - retinitis pigmentosa RGO:35181 ORDO:247794 RGO:35182 juvenile cataract - microcornea - renal glucosuria RGO:35182 HP:0001118 SNOMEDCT:399336001 RGO:35183 juvenile cataract RGO:35183 SNOMEDCT:267430007 RGO:35184 renal glucosuria RGO:35184 EDSS EDSS1 ORDO:247820 RGO:35185 ectodermal dysplasia - syndactyly syndrome RGO:35185 EDSS2 ORDO:247827 RGO:35188 ectodermal dysplasia - cutaneous syndactyly syndrome RGO:35188 HP:0012725 RGO:35189 cutaneous syndactyly RGO:35189 ORDO:251279 RGO:35192 microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen RGO:35192 HP:0012152 RGO:35193 foveoschisis RGO:35193 HP:0012426 SNOMEDCT:33629003 RGO:35194 optic disc drusen RGO:35194 HbS - beta-thalassemia ORDO:251359 RGO:35195 sickle cell - beta-thalassemia disease RGO:35195 HbSC disease ORDO:251365 RGO:35197 sickle cell - hemoglobin C disease RGO:35197 HbSD disease ORDO:251370 RGO:35199 sickle cell - hemoglobin D disease RGO:35199 DOID:5378 SNOMEDCT:66729008 RGO:35200 hemoglobin D disease RGO:35200 HbSE disease ORDO:251375 RGO:35202 sickle cell - hemoglobin E disease RGO:35202 DOID:5379 SNOMEDCT:25065001 RGO:35203 hemoglobin E disease RGO:35203 HPFH - sickle cell disease ORDO:251380 RGO:35205 hereditary persistence of fetal hemoglobin - sickle cell disease RGO:35205 hyperzincemia and hypercalprotectinemia ORDO:251523 RGO:35207 recurrent infections - inflammatory syndrome due to zinc metabolism disorder RGO:35207 RGO:35208 recurrent infection RGO:35208 RGO:35209 inflammatory syndrome RGO:35209 RGO:35210 zinc metabolism disorder RGO:35210 SPAX4 autosomal recessive spastic ataxia type 4 ORDO:254343 RGO:35212 autosomal recessive spastic ataxia - optic atrophy - dysarthria RGO:35212 hearing loss - encephaloneuropathy - obesity - valvulopathy ORDO:254898 RGO:35215 deafness - encephaloneuropathy - obesity - valvulopathy RGO:35215 RGO:35216 encephaloneuropathy RGO:35216 RGO:35217 valvulopathy RGO:35217 ORDO:254902 RGO:35219 renal tubulopathy - encephalopathy - liver failure RGO:35219 RGO:35220 renal tubulopathy RGO:35220 ORDO:261559 RGO:35221 blepharophimosis - epicanthus inversus - ptosis due to 3q23 microdeletion RGO:35221 RGO:35222 3q23 microdeletion RGO:35222 ORDO:261572 RGO:35223 blepharophimosis - epicanthus inversus - ptosis due to a point mutation RGO:35223 ORDO:261579 RGO:35224 blepharophimosis - epicanthus inversus - ptosis due to polyA expansion RGO:35224 ORDO:263410 RGO:35225 infantile spasms - psychomotor retardation - progressive brain atrophy - basal ganglia disease RGO:35225 RGO:35226 progressive brain atrophy RGO:35226 LGMD2P ORDO:280333 RGO:35227 autosomal recessive limb-girdle muscular dystrophy - dystroglycanopathy type C7 RGO:35227 RGO:35228 dystroglycanopathy type C7 RGO:35228 IDMDC ORDO:280384 RGO:35230 recessive intellectual disability - motor dysfunction - multiple joint contractures RGO:35230 RADLEX:RID5238 SNOMEDCT:52559000 RGO:35231 motor dysfunction RGO:35231 HP:0002828 RGO:35232 multiple joint contractures RGO:35232 ORDO:280633 RGO:35234 multiple congenital anomalies - hypotonia - seizures syndrome RGO:35234 syndromic Moyamoya disease ORDO:280679 RGO:35235 moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism RGO:35235 SCAR11 autosomal recessive spinocerebellar ataxia type 11 ORDO:284271 RGO:35238 autosomal recessive cerebellar ataxia - psychomotor retardation RGO:35238 Autosomal recessive spinocerebellar ataxia 12 SCAR12 ORDO:284282 RGO:35241 autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit RGO:35241 Loeys-Dietz syndrome with osteoarthritis ORDO:284984 RGO:35244 aneurysm - osteoarthritis syndrome RGO:35244 PASH syndrome ORDO:289478 RGO:35247 pyoderma gangrenosum - acne - suppurative hidradenitis RGO:35247 ORDO:289483 RGO:35249 intellectual deficit - alacrima - achalasia RGO:35249 ORDO:289553 RGO:35250 dysmorphism - conductive hearing loss - heart defect RGO:35250 ROHHAD rapid-onset childhood obesity - hypothalamic dysfunction-hypoventilation-autonomic dysregulation - neural tumors ORDO:293987 RGO:35251 rapid-onset childhood obesity - hypothalamic dysfunction - hypoventilation - autonomic dysregulation syndrome RGO:35251 RGO:35252 rapid-onset childhood obesity RGO:35252 SNOMEDCT:111568001 RGO:35253 hypothalamic dysfunction RGO:35253 HP:0002271 RGO:35254 autonomic dysregulation RGO:35254 autosomal dominant ectodermal dysplasia - cancer predisposition syndrome ORDO:300576 RGO:35257 oligodontia - cancer predisposition syndrome RGO:35257 RGO:35258 cancer predisposition RGO:35258 ORDO:314041 RGO:35260 marfanoid habitus - inguinal hernia - advanced bone age RGO:35260 LTBL ORDO:314051 RGO:35261 leukoencephalopathy - thalamus and brainstem anomalies - high lactate RGO:35261 RGO:35262 thalamus anomaly RGO:35262 RGO:35263 high lactate RGO:35263 RGO:35264 brainstem anomaly RGO:35264 ORDO:319678 RGO:35266 encephalopathy - hypertrophic cardiomyopathy - renal tubular disease RGO:35266 HP:0000124 RGO:35267 renal tubular disease RGO:35267 tall stature - scoliosis - macrodactyly of the halluces ORDO:329191 RGO:35268 tall stature - scoliosis - macrodactyly of the great toes RGO:35268 RGO:35269 macrodactyly of the great toes RGO:35269 congenital muscular dystrophy - muscle hypertrophy - intellectual deficit due to POMT1 ORDO:329206 RGO:35271 congenital muscular dystrophy - muscle hypertrophy - severe intellectual deficit RGO:35271 HP:0003712 SNOMEDCT:249829006 RGO:35272 muscle hypertrophy RGO:35272 ORDO:329252 RGO:35274 spondylocostal dysostosis - hypospadias - intellectual deficit RGO:35274 ORDO:329475 RGO:35275 spastic paraplegia - Paget disease of bone RGO:35275 HbLepore - beta-thalassemia Lepore - beta-thalassemia ORDO:330032 RGO:35276 hemoglobin Lepore - beta-thalassemia RGO:35276 SNOMEDCT:103236006 RGO:35277 hemoglobin Lepore RGO:35277 ORDO:330054 RGO:35280 congenital cataract - progressive muscular hypotonia - hearing loss - developmental delay RGO:35280 RGO:35281 progressive muscular hypotonia RGO:35281 congenital ichthyosis - intellectual deficit - spastic tetraplegia ORDO:352333 RGO:35282 congenital ichthyosis - intellectual deficit - spastic quadriplegia RGO:35282 PEO - myopathy - emaciation mtDNA maintenance syndrome due to MGME1 deficiency ORDO:352447 RGO:35284 progressive external ophthalmoplegia - myopathy - emaciation RGO:35284 DOID:12558 HP:0000590 ICD10CM:H49.4 SNOMEDCT:46252003 RGO:35285 progressive external ophthalmoplegia RGO:35285 RGO:35286 emaciation RGO:35286 ORDO:352487 RGO:35289 digital anomalies - intellectual deficit - short stature RGO:35289 autosomal recessive intellectual deficit due to TRAPPC9 deficiency ORDO:352530 RGO:35290 intellectual deficit - obesity - brain malformations - facial dysmorphism RGO:35290 Bainbridge-Roppers syndrome ORDO:352577 RGO:35292 severe feeding difficulties - failure to thrive - microcephaly due to ASXL3 deficiency RGO:35292 RGO:35293 severe feeding difficulties RGO:35293 RGO:35294 ASXL3 deficiency RGO:35294 focal epilepsy - intellectual deficit - dysarthria - ataxia ORDO:352587 RGO:35296 focal epilepsy - intellectual deficit - cerebro-cerebellar malformation RGO:35296 RGO:35297 cerebro-cerebellar malformation RGO:35297 ORDO:352654 RGO:35299 early-onset progressive neurodegeneration - blindness - ataxia - spasticity RGO:35299 RGO:35300 early-onset progressive neurodegeneration RGO:35300 FILS syndrome ORDO:352712 RGO:35301 facial dysmorphism - immunodeficiency - livedo - short stature RGO:35301 SNOMEDCT:247478000 RGO:35302 livedo RGO:35302 ORDO:356996 RGO:35304 intellectual deficit - hypotonia - spasticity - sleep disorder RGO:35304 DOID:535 SNOMEDCT:39898005 RGO:35305 sleep disorder RGO:35305 macroblepharon - ectropion - hypertelorism - macrostomia syndrome ORDO:357158 RGO:35306 mandibulofacial dysostosis - macroblepharon - macrostomia RGO:35306 RGO:35307 macroblepharon RGO:35307 ORDO:357175 RGO:35309 short ulna - dysmorphism - hypotonia - intellectual deficit RGO:35309 ORDO:357329 RGO:35310 cryptosporidiosis - chronic cholangitis - liver disease RGO:35310 DOID:9439 SNOMEDCT:71912000 RGO:35311 chronic cholangitis RGO:35311 Wahab syndrome ORDO:357332 RGO:35312 syndactyly - camptodactyly and clinodactyly of fifth fingers - bifid toes RGO:35312 RGO:35313 camptodactyly and clinodactyly of fifth fingers RGO:35313 RGO:35314 bifid toes RGO:35314 ORDO:340 RGO:35316 hemorrhagic fever - renal syndrome RGO:35316 RGO:35317 hantavirus fever RGO:35317 RGO:35321 hemorrhagic vascular metastasis RGO:35321 RGO:35322 heroin abuse RGO:35322 RGO:35323 saprophytic fungal infection RGO:35323 RGO:35325 normal reduction in amniotic fluid late in pregnancy RGO:35325 SNOMEDCT:59634004 RGO:35326 postmaturity RGO:35326 SNOMEDCT:276654001 RGO:35327 fetal malformation RGO:35327 RGO:35328 kidney obstruction RGO:35328 RGO:35329 bladder obstruction RGO:35329 RADLEX:RID4379 SNOMEDCT:54443001 RGO:35331 fibrous mesothelioma RGO:35331 RGO:35332 Brunn nests RGO:35332 RGO:35333 gelatinous plug RGO:35333 RGO:35334 trigonal polyp RGO:35334 RGO:35335 prolapsing ectopic ureterocele RGO:35335 RGO:35336 vaginal leiomyoma RGO:35336 RGO:35337 vaginal fibroma RGO:35337 RGO:35338 prostatic lymphomatosis RGO:35338 RGO:35339 prostatic lymphoma RGO:35339 RGO:35340 prostatic hemangiopericytoma RGO:35340 RGO:35341 prostatic rhabdomyosarcoma RGO:35341 RGO:35342 leiomyoma of lower uterine segment RGO:35342 RGO:35343 idiopathic tracheobrochial cartilage calcification RGO:35343 RGO:35344 carotid arteritis RGO:35344 RGO:35345 bacterial arteritis RGO:35345 RGO:35346 infectious aneurysm RGO:35346 RGO:35347 ergot poisoning RGO:35347 RGO:35348 high-flow angiopathy RGO:35348 RGO:35349 fungal arteritis RGO:35349 RGO:35350 viral arteritis RGO:35350 DOID:8536 SNOMEDCT:4740000 RGO:35351 herpes zoster infection RGO:35351 RGO:35352 chronic bronchopleural fistula RGO:35352 HP:0011109 ICD10CM:J32 SNOMEDCT:40055000 RGO:35353 chronic sinusitis RGO:35353 pulmonary carcinoid RGO:35354 lung carcinoid RGO:35354 DOID:786 RGO:35355 laryngeal disease RGO:35355 RGO:35362 chest wall abnormality RGO:35362 HP:0001555 RGO:35363 asymmetric chest RGO:35363 RGO:35364 congenital rib anomaly RGO:35364 RGO:35365 congenital spinal anomaly RGO:35365 RGO:35366 fusion of posterior vertebral elements RGO:35366 RGO:35367 unilateral spinal bar RGO:35367 RGO:35368 vertebral segmentation anomaly RGO:35368 RGO:35369 wedge vertebra RGO:35369 RGO:35371 paraspinous muscle spasm RGO:35371 RGO:35372 psoas hemorrhage RGO:35372 HP:0001269 SNOMEDCT:20022000 RGO:35373 hemiparesis RGO:35373 RGO:35374 leg shortening RGO:35374 RGO:35375 leg amputation RGO:35375 RGO:35376 familial congenital partial atresia of the larynx RGO:35376 RGO:35378 flattened or inverted diaphragm RGO:35378 RGO:35379 dilated airway distal to the obstruction RGO:35379 SNOMEDCT:3218000 RGO:35381 fungus infection RGO:35381 RGO:35382 infected urinoma RGO:35382 SNOMEDCT:698573001 RGO:35383 infected hematoma RGO:35383 RGO:35384 removal of ureteral calculus RGO:35384 RGO:35386 extraurinary infection RGO:35386 RGO:35387 trauma to ureter RGO:35387 RGO:35388 trauma to kidney RGO:35388 RGO:35389 Charcot spine RGO:35389 RGO:35390 neuropathic osteoarthropathy RGO:35390 RGO:35391 spina bifida with meningocele RGO:35391 RGO:35392 bony spinal bar RGO:35392 RGO:35393 vertebral dislocation RGO:35393 RGO:35394 spine neoplasm RGO:35394 SNOMEDCT:249858009 RGO:35395 bad posture RGO:35395 RGO:35396 hammered silver skull RGO:35396 RGO:35397 beaten silver skull RGO:35397 ICD10CM:J38.5 SNOMEDCT:406444002 RGO:35398 laryngeal spasm RGO:35398 SNOMEDCT:387358007 SNOMEDCT:65026000 RGO:35399 ephedrine RGO:35399 RGO:35402 intraluminal mass RGO:35402 RGO:35403 intraluminal clots RGO:35403 RGO:35404 intraluminal calculus RGO:35404 RGO:35405 intraluminal fungus ball RGO:35405 RGO:35406 perforated gallbladder RGO:35406 SNOMEDCT:262846002 RGO:35407 duodenal rupture RGO:35407 RGO:35408 colonic rupture RGO:35408 SNOMEDCT:54686006 RGO:35409 rectal biopsy RGO:35409 RGO:35410 needle aspiration RGO:35410 RGO:35411 perforation of gastrointestinal tract RGO:35411 aorticoiliac steno-occlusion RGO:35413 small aorta syndrome RGO:35413 SNOMEDCT:58437007 RGO:35415 tuberculosis of meninges RGO:35415 RGO:35416 nonfunctioning kidney RGO:35416 HP:0000104 SNOMEDCT:249582007 RGO:35417 absent kidney RGO:35417 SNOMEDCT:38822007 RGO:35418 bladder infection RGO:35418 RGO:35419 chemotherapy-induced cystitis RGO:35419 RGO:35420 irritative contrast medium RGO:35420 RGO:35421 intraparotid lymph node RGO:35421 DOID:1681 RADLEX:RID3274 RGO:35422 septal defect RGO:35422 RGO:35423 primary malignant bone neoplasm RGO:35423 RGO:35424 vertebral body underdevelopment RGO:35424 RGO:35425 supraglottic web RGO:35425 RGO:35426 glottic web RGO:35426 SNOMEDCT:444921008 RGO:35427 subglottic web RGO:35427 RGO:35432 active osteoporosis RGO:35432 RGO:35433 noxious gas inhalation RGO:35433 RGO:35434 dinitrogen tetroxide RGO:35434 RADLEX:RID5076 RGO:35436 spur RGO:35436 SNOMEDCT:29506000 RGO:35437 boxing RGO:35437 RGO:35438 progressive muscular wasting RGO:35438 RGO:35442 cranial suture diastasis RGO:35442 RGO:35443 deep interdigitation of cranial sutures RGO:35443 RGO:35444 isolated clinodactyly of fifth finger RGO:35444 RGO:35445 thin hands RGO:35445 RGO:35446 thin feet RGO:35446 RGO:35447 colonic aganglionosis RGO:35447 HP:0008905 RGO:35449 rhizomelia RGO:35449 RGO:35451 laryngeal agenesis RGO:35451 RGO:35452 congenital atresia of stomach RGO:35452 SNOMEDCT:51118003 RGO:35453 congenital atresia of duodenum RGO:35453 RGO:35454 congenital atresia of small bowel RGO:35454 SNOMEDCT:37054000 RGO:35455 congenital atresia of colon RGO:35455 SNOMEDCT:91375006 RGO:35456 congenital atresia of rectum RGO:35456 DOID:10488 SNOMEDCT:204712000 RGO:35457 congenital atresia of anus RGO:35457 SNOMEDCT:93387008 RGO:35458 congenital stenosis of stomach RGO:35458 SNOMEDCT:16376000 RGO:35459 congenital stenosis of duodenum RGO:35459 RGO:35460 congenital stenosis of small bowel RGO:35460 SNOMEDCT:253769003 RGO:35461 congenital stenosis of colon RGO:35461 RGO:35462 congenital stenosis of rectum RGO:35462 RGO:35463 congenital stenosis of anus RGO:35463 three testes three testicles tritestes RGO:35472 triorchidism RGO:35472 ORDO:2837 RGO:35479 pellagra-like skin rash - neurological manifestations RGO:35479 RGO:35480 pellagra-like skin rash RGO:35480 RGO:35483 classic galactosemia RGO:35483 RGO:35524 hypodactyly RGO:35524 pleuropulmonary blastoma family tumor and dysplasia syndrome SNOMEDCT:702411003 RGO:35526 DICER1 syndrome RGO:35526 RADLEX:RID34426 SNOMEDCT:168836005 RGO:35531 barium enema RGO:35531 portal venous thrombosis DOID:11695 HP:0030242 ICD10CM:I81 SNOMEDCT:17920008 RGO:35534 portal vein thrombosis RGO:35534 SNOMEDCT:57348003 RGO:35535 portal vein obstruction RGO:35535 renal transplant renal transplantation transplanted kidney SNOMEDCT:70536003 RGO:35542 kidney transplant RGO:35542 RGO:35561 idiopathic adrenal calcification RGO:35561 RGO:35562 adrenal abscess RGO:35562 DOID:2533 RGO:35563 splenic infarct RGO:35563 RGO:35564 testicular hematoma RGO:35564 DOID:5104 SNOMEDCT:33793000 RGO:35565 testicular infarct RGO:35565 torsion of epididymis RGO:35566 epididymal torsion RGO:35566 RADLEX:RID4813 SNOMEDCT:129256008 SNOMEDCT:51795009 RGO:35567 torsion RGO:35567 RGO:35571 epididymal abscess RGO:35571 DOID:3883 SNOMEDCT:716318002 RGO:35573 Lynch syndrome RGO:35573 DOID:9256 RADLEX:RID45684 RGO:35576 colorectal cancer RGO:35576 sarcoma of spleen RGO:35577 splenic sarcoma RGO:35577 RGO:35595 adrenal biopsy RGO:35595 RGO:35596 abdominal trauma RGO:35596 DOID:11240 RGO:35598 appendiceal neoplasm RGO:35598 RGO:35599 appendiceal carcinoma RGO:35599 RGO:35600 neoplasm of papilla of Vater RGO:35600 RGO:35602 bile duct neoplasm RGO:35602 RGO:35605 small bowel polyp RGO:35605 RGO:35606 small bowel neoplasm RGO:35606 RGO:35607 small bowel metastasis RGO:35607 RGO:35608 superior ophthalmic vein varix RGO:35608 RGO:35609 colonic varix RGO:35609 RADLEX:RID3372 RGO:35610 ovarian vein varix RGO:35610 RGO:35611 abdominal venous varix RGO:35611 RGO:35613 duodenal varix RGO:35613 HP:0030169 SNOMEDCT:91109007 RGO:35614 gastric varix RGO:35614 RGO:35615 gallbladder varix RGO:35615 RGO:35616 joint vein varix RGO:35616 DOID:112 HP:0002040 SNOMEDCT:28670008 RGO:35617 esophageal varix RGO:35617 RGO:35618 small bowel varix RGO:35618 RGO:35619 intracranial varix RGO:35619 DOID:799 RADLEX:RID3366 SNOMEDCT:12856003 RGO:35621 varix RGO:35621 RGO:35622 site-specific avascular necrosis RGO:35622 RGO:35637 bilateral vestibular schwannoma RGO:35637 RGO:35638 bilateral acoustic neuroma RGO:35638 RGO:35725 HbSS disease RGO:35725 RGO:35734 spontaneous abortion RGO:35734 RGO:35735 miscarriage RGO:35735 M. avium-intracellulare MAI Mycobacterium avium-intercellulare Mycobacterium avium-intracellulare RGO:35739 Mycobacterium avium-intracellulare infection RGO:35739 RGO:35740 Mycobacterium avium complex RGO:35740 proteinaceous cyst RGO:35746 proteinaceous renal cyst RGO:35746